Edgar Filing: NEUROLOGIX INC/DE

10-Q

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

(Mark One)


þ		QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarter ended June 30, 2010


o		TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from to

Commission File Number: 000-13347

NEUROLOGIX, INC.

(Exact name of Registrant as specified in its charter)


Delaware		06-1582875

(State or other jurisdiction		(I.R.S. Employer Identification No.)
of incorporation or organization)

One Bridge Plaza, Fort Lee, NJ 07024

(Address of principal executive offices)

(201) 592-6451

(Registrant’s telephone number, including area code)

Indicate by check mark whether the Registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the Registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes þ No o

Indicate by check mark whether the Registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the Registrant was required to submit and post such files). Yes o No o

Indicate by check mark whether the Registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See definition of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check one):


Large accelerated filer o	Accelerated filer o	Non-accelerated filer o	Smaller reporting company þ
		(Do not check if a smaller reporting company)

Indicate by check mark whether the Registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes o No þ

As of August 10, 2010, 27,865,010 shares of common stock were outstanding.

TABLE OF CONTENTS


	Page

PART I. FINANCIAL INFORMATION

Item 1. Financial Statements

Balance Sheets (Unaudited)		4

Statements of Operations (Unaudited)		5

Statements of Changes in Stockholders’ Equity (Deficiency) (Unaudited)		6

Statements of Cash Flows (Unaudited)		10

Notes to Financial Statements (Unaudited)		12

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations		20

Item 3. Quantitative and Qualitative Disclosures About Market Risk		25

Item 4. Controls and Procedures		26

PART II. OTHER INFORMATION		26

Item 6. Exhibits		26

Exhibit 31.1
Exhibit 31.2
Exhibit 32.1

NEUROLOGIX, INC.
(A Development Stage Company)

BALANCE SHEETS

(Amounts in thousands, except share and per share amounts)


	June 30,			December 31,
	2010			2009
	(Unaudited)
ASSETS
Current assets:
Cash and cash equivalents	$	4,512		$	9,637
Prepaid expenses and other current assets		177			395

Total current assets		4,689			10,032
Equipment, less accumulated depreciation of $659 and $624 at June 30, 2010 and December 31, 2009, respectively		94			129
Intangible assets, less accumulated amortization of $308 and $262 at June 30, 2010 and December 31, 2009, respectively		973			891
Other assets		5			5

Total assets	$	5,761		$	11,057


LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Accounts payable and accrued expenses	$	1,473		$	1,834

Total current liabilities		1,473			1,834

Derivative financial instruments, at estimated fair value — warrants		6,435			3,847

Total liabilities		7,908			5,681


Commitments and contingencies
Stockholders’ equity:
Preferred stock; 5,000,000 shares authorized
Series A — Convertible, $0.10 par value; 650 shares designated, 645 shares issued and outstanding at June 30, 2010 and December 31, 2009, with an aggregate liquidation preference of $1		—			—
Series C — Convertible, $0.10 par value; 700,000 shares designated, 281,263 shares issued and outstanding at June 30, 2010 and December 31, 2009, with an aggregate liquidation preference of $8,630 and $7,008 at June 30, 2010 and December 31, 2009, respectively		28			28
Series D — Convertible, $0.10 par value; 792,100 shares designated, 734,898 shares issued and outstanding at June 30, 2010 and December 31, 2009, with an aggregate liquidation preference of $32,928 and $29,420 at June 30, 2010 and December 31, 2009, respectively		73			73
Common Stock:
$0.001 par value; 100,000,000 shares authorized, 27,865,010 shares issued and outstanding at each of June 30, 2010 and December 31, 2009		28			28
Additional paid-in capital		57,221			56,775
Deficit accumulated during the development stage		(59,497	)		(51,528	)

Total stockholders’ equity		(2,147	)		5,376

Total liabilities and stockholders’ equity	$	5,761		$	11,057

See accompanying notes to financial statements.

NEUROLOGIX, INC.
(A Development Stage Company)

STATEMENTS OF OPERATIONS

(UNAUDITED)

(Amounts in thousands, except share and per share amounts)


													For the period
													February 12, 1999
	Six Months Ended June 30,						Three Months Ended June 30,						(inception) through
	2010			2009			2010			2009			June 30, 2010
Revenues	$	—		$	—		$	—		$	—		$	—
Operating expenses:
Research and development		3,399			3,658			1,542			2,249			30,860
General and administrative expenses		1,983			1,548			699			799			20,980

Loss from operations		(5,382	)		(5,206	)		(2,241	)		(3,048	)		(51,840	)


Other income (expense):
Dividend, interest and other income		1			49			1			16			1,884
Interest expense-related parties		—			—			—			—			(411	)
Change in estimated fair value of derivative financial instruments — warrants		(2,588	)		(1,980	)		(2,232	)		809			(5,365	)

Other (expense) income, net		(2,587	)		(1,931	)		(2,231	)		825			(3,892	)

Net loss		(7,969	)		(7,137	)		(4,472	)		(2,223	)	$	(55,732	)


Preferred stock dividends		(1,558	)		(1,451	)		(787	)		(734	)

Net loss applicable to common stock	$	(9,527	)	$	(8,588	)	$	(5,259	)	$	(2,957	)


Net loss applicable to common stock per share, basic and diluted	$	(0.34	)	$	(0.31	)	$	(0.19	)	$	(0.11	)


Weighted average common shares outstanding, basic and diluted		27,865,010			27,795,850			27,865,010			27,827,292

See accompanying notes to financial statements.

NEUROLOGIX, INC.
(A Development Stage Company)

STATEMENTS OF CHANGES IN STOCKHOLDERS’ EQUITY (DEFICIENCY)

FOR THE PERIOD FROM FEBRUARY 12, 1999 (INCEPTION) THROUGH JUNE 30, 2010

(UNAUDITED)

(Amounts in thousands, except for share and per share amounts)


																				Deficit
																				Accumulated
														Additional						During the
	Series D Preferred Stock				Series C Preferred Stock				Common Stock					Paid-in			Unearned			Development
	Shares		Amount		Shares		Amount		Shares			Amount		Capital			Compensation			Stage			Total

Sale of common stock to founders		—	$	0		—	$	0		6,004,146		$	0	$	4		$	0		$	0		$	4
Net loss		—		—		—		—		—			—		—			—			(328	)		(328	)
Balance, December 31, 1999		—	$	0		—	$	0		6,004,146		$	0	$	4		$	0		$	(328	)	$	(324	)
Net loss		—		—		—		—		—			—		—			—			(1,055	)		(1,055	)
Balance, December 31, 2000		—	$	0		—	$	0		6,004,146		$	0	$	4		$	0		$	(1,383	)	$	(1,379	)
Stock options granted for services		—		—		—		—		—			—		9			—			—			9
Common stock issued for intangible assets at $0.09 per share		—		—		—		—		259,491			—		24			—			—			24
Net loss		—		—		—		—		—			—		—			—			(870	)		(870	)
Balance, December 31, 2001		—	$	0		—	$	0		6,263,637		$	0	$	37		$	0		$	(2,253	)	$	(2,216	)
Retirement of founder shares		—		—		—		—		(33,126	)		—		—			—			—			—
Common Stock issued pursuant to license agreement at $1.56 per share		—		—		—		—		368,761			—		577			(577	)		—			—
Private placement of Series B convertible preferred stock		—		—		—		—		—			—		2,613			—			—			2,613
Amortization of unearned compensation		—		—		—		—		—			—		—			24			—			24
Net loss		—		—		—		—		—			—		—			—			(1,310	)		(1,310	)
Balance, December 31, 2002		—	$	0		—	$	0		6,599,272		$	0	$	3,227		$	(553	)	$	(3,563	)	$	(889	)
Sale of Common Stock		—		—		—		—		276,054			—		90			(89	)		—			1
Amortization of unearned compensation		—		—		—		—		—			—		—			164			—			164
Net loss		—		—		—		—		—			—		—			—			(2,274	)		(2,274	)
Balance, December 31, 2003		—	$	0		—	$	0		6,875,326		$	0	$	3,317		$	(478	)	$	(5,837	)	$	(2,998	)
Conversion of note payable to Common Stock at $2.17 per share		—		—		—		—		1,091,321			1		2,371			—			—			2,372
Conversion of mandatory redeemable preferred stock to Common Stock		—		—		—		—		6,086,991			6		494			—			—			500
Conversion of Series B convertible preferred stock to Common Stock		—		—		—		—		1,354,746			1		(1	)		—			—			—
Effects of reverse acquisition		—		—		—		—		7,103,020			14		5,886			—			—			5,900
Amortization of unearned compensation		—		—		—		—		—			—		—			202			—			202

NEUROLOGIX, INC.
(A Development Stage Company)
STATEMENTS OF CHANGES IN STOCKHOLDERS’ EQUITY (DEFICIENCY)
FOR THE PERIOD FROM FEBRUARY 12, 1999 (INCEPTION) THROUGH JUNE 30, 2010
(UNAUDITED)
(Amounts in thousands, except for share and per share amounts)


																			Deficit
																			Accumulated
													Additional						During the
	Series D Preferred Stock				Series C Preferred Stock				Common Stock				Paid-in			Unearned			Development
	Shares		Amount		Shares		Amount		Shares		Amount		Capital			Compensation			Stage			Total

Stock options granted for services		—		—		—		—		—		—		42			(42	)		—			—
Exercise of stock options		—		—		—		—		10,000		—		15			—			—			15
Net loss		—		—		—		—		—		—		—			—			(2,937	)		(2,937	)
Balance, December 31, 2004		—	$	0		—	$	0		22,521,404	$	22	$	12,124		$	(318	)	$	(8,774	)	$	3,054
Sale of Common Stock through private placement at an average price of $1.30 per share		—		—		—		—		2,473,914		4		3,062			—			—			3,066
Sale of Common Stock at an average price of $1.752 per share and warrants to Medtronic		—		—		—		—		1,141,552		1		2,794			—			—			2,795
Amortization of unearned compensation		—		—		—		—		—		—		—			825			—			825
Stock options granted for services		—		—		—		—		—		—		1,305			(1,305	)		—			—
Exercise of stock options		—		—		—		—		406,054		—		127			—			—			127
Net loss		—		—		—		—		—		—		—			—			(5,345	)		(5,345	)
Balance, December 31, 2005		—	$	0		—	$	0		26,542,924	$	27	$	19,412		$	(798	)	$	(14,119	)	$	4,522
Sale of Preferred Stock through private placement at an average price of $35.00 per share		—		—		342,857		34		—		—		11,578			—			—			11,612
Fair value of beneficial conversion rights issued in connection with issuance of Series C Preferred Stock		—		—		—		—		—		—		2,621			—			—			2,621
Preferred Dividend and accretion of fair value of beneficial conversion charge		—		—		25,298		3		—		—		(3	)		—			(2,621	)		(2,621	)
Employee share-based compensation expense		—		—		—		—		—		—		1,193			—			—			1,193
Non-employee share-based compensation		—		—		—		—		—		—		83			—			—			83
Reclassification of prior year non-employee compensation to prepaid expenses		—		—		—		—		—		—		—			487			—			487
Effects of adoption of ASC Topic 718		—		—		—		—		—		—		(311	)		311			—			—
Net loss		—		—		—		—		—		—		—			—			(7,046	)		(7,046	)
Balance, December 31, 2006		—	$	0		368,155	$	37		26,542,924	$	27	$	34,573		$	0		$	(23,786	)	$	10,851
Sale of Series D Preferred Stock through private placement at an average price of $35.00 per share		428,571		43		—		—		—		—		14,727			—			—			14,770


																						Deficit
																						Accumulated
																	Additional					During the
	Series D Preferred Stock						Series C Preferred Stock						Common Stock				Paid-in			Unearned		Development
	Shares			Amount			Shares			Amount			Shares		Amount		Capital			Compensation		Stage			Total

Fair value of beneficial conversion rights issued in connection with the issuance of Series D Preferred Stock		—			—			—			—			—		—		2,130			—		—			2,130
Preferred Dividend and accretion of fair value of beneficial conversion charge		5,108			1			68,801			7			—		—		(8	)		—		(2,130	)		(2,130	)
Contingent beneficial conversion feature related to Series C Preferred Stock		—			—			—			—			—		—		627			—		(627	)		—
Induced conversion of preferred stock in connection with the issuance of Series D Preferred Stock		163,470			16			(230,184	)		(23	)		—		—		(347	)		—		354			—
Issuance of Series C Preferred Stock in connection with induced conversion of preferred stock		—			—			93,940			9			—		—		2,949			—		(2,958	)		—
Issuance of Common Stock in connection with issuance of Series D Preferred Stock		—			—			—			—			192,017		—		192			—		(192	)		—
Employee share-based compensation expense		—			—			—			—			—		—		702			—		—			702
Non-employee share-based compensation		—			—			—			—			—		—		72			—		—			72
Conversion of Series C Preferred Stock to Common Stock		—			—			(5,597	)		—			110,052		—		—			—		—			—
Exercise of stock options		—			—			—			—			787,815		1		590			—		—			591
Net loss		—			—			—			—			—		—		—			—		(6,817	)		(6,817	)
Balance, December 31, 2007		597,149		$	60			295,115		$	30			27,632,808	$	28	$	56,207		$	0	$	(36,156	)	$	20,169
Sale of Series D Preferred Stock through private placement at an average price of $35.00 per share		142,857			14			—			—			—		—		4,918			—		—			4,932
Fair value of beneficial conversion rights issued in connection with the issuance of Series D Preferred Stock		—			—			—			—			—		—		562			—		—			562
Accretion of fair value of beneficial conversion charge		—			—			—			—			—		—		—			—		(562	)		(562	)
Contingent beneficial conversion feature related to Series C Preferred Stock		—			—			—			—			—		—		212			—		(212	)		—
Adjustment to preferred dividends accrued		(5,108	)		(1	)		(3,237	)		(1	)		—		—		2			—		—			—


																				Deficit
																				Accumulated
															Additional					During the
	Series D Preferred Stock				Series C Preferred Stock						Common Stock				Paid-in			Unearned		Development
	Shares		Amount		Shares			Amount			Shares		Amount		Capital			Compensation		Stage			Total

Employee share-based compensation expense		—		—		—			—			—		—		489			—		—			489
Non-employee share-based compensation		—		—		—			—			—		—		3			—		—			3
Conversion of Series C Preferred Stock to Common Stock		—		—		(6,000	)		—			131,250		—		—			—		—			—
Net Loss		—		—		—			—			—		—		—			—		(6,320	)		(6,320	)
Balance December 31, 2008		734,898	$	73		285,878		$	29			27,764,058	$	28	$	62,393		$	0	$	(43,250	)	$	19,273
Employee share-based compensation expense		—		—		—			—			—		—		448			—		—			448
Non-employee share-based compensation		—		—		—			—			—		—		185			—		—			185
Cumulative effect of adoption of ASC Topic 815-40		—		—		—			—			—		—		(6,252	)		—		5,183			(1,069	)
Conversion of Series C Preferred Stock to Common Stock		—		—		(4,615	)		(1	)		100,952		—		1			—		—			—
Net Loss		—		—		—			—			—		—		—			—		(13,461	)		(13,461	)
Balance December 31, 2009		734,898	$	73		281,263		$	28			27,865,010	$	28	$	56,775		$	0	$	(51,528	)	$	5,376
Employee share-based compensation expense		—		—		—			—			—		—		367			—		—			367
Non-employee share-based compensation		—		—		—			—			—		—		79			—		—			79
Net Loss		—		—		—			—			—		—		—			—		(7,969	)		(7,969	)

Balance June 30, 2010		734,898	$	73		281,263		$	28			27,865,010	$	28	$	57,221		$	0	$	(59,497	)	$	(2,147	)

See accompanying notes to financial statements.

NEUROLOGIX, INC.
(A Development Stage Company)

STATEMENTS OF CASH FLOWS

(UNAUDITED)

(Amounts in thousands)


							For the period
							February
							12, 1999 (inception)
	Six Months Ended June 30,						through
	2010			2009			June 30, 2010
Operating activities:
Net loss	$	(7,969	)	$	(7,137	)	$	(55,732	)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation		35			42			665
Amortization		46			40			448
Gain on redemption of investment		—			—			(62	)
Stock options granted for services		—			—			9
Impairment of intangible assets		—			—			199
Amortization of non-employee share-based compensation		93			132			1,800
Share-based employee compensation expense		367			305			3,199
Non-cash interest expense		—			—			378
Change in estimated fair value of derivative financial instruments — warrants		2,588			1,980			5,365
Changes in operating assets and liabilities
Decrease (increase) in prepaid expenses and other current assets		204			(13	)		742
(Decrease) increase in accounts payable and accrued expenses		(361	)		638			1,413

Net cash used in operating activities		(4,997	)		(4,013	)		(41,576	)

Investing activities:
Security deposits paid		—			—			(7	)
Purchases of equipment		—			(29	)		(645	)
Additions to intangible assets		(128	)		(128	)		(1,590	)
Proceeds from redemption of investment		—			—			65
Purchases of marketable securities		—			—			(12,673	)
Proceeds from maturities of marketable securities		—			—			12,673

Net cash used in investing activities		(128	)		(157	)		(2,177	)

Financing activities:
Proceeds from note payable		—			—			1,100
Borrowings from related party		—			—			2,000
Cash acquired in Merger		—			—			5,413
Merger-related costs		—			—			(375	)
Payments of capital lease obligations		—			—			(99	)
Proceeds from exercise of stock options		—			—			733
Proceeds from issuance of common stock and warrants		—			—			5,066
Proceeds from issuance of preferred stock		—			—			34,427

Net cash provided by financing activities		—			—			48,265

Net (decrease) increase in cash and cash equivalents		(5,125	)		(4,170	)		4,512
Cash and cash equivalents, beginning of period		9,637			18,906			—

NEUROLOGIX, INC.
(A Development Stage Company)
STATEMENTS OF CASH FLOWS
(UNAUDITED)
(Amounts in thousands)


					For the period
					February
					12, 1999 (inception)
	Six Months Ended June 30,				through
	2010		2009		June 30, 2010
Cash and cash equivalents, end of period	$	4,512	$	14,736	$	4,512

Supplemental disclosure of non-cash investing and financing activities:
Dividends on Series C Preferred Stock paid in preferred shares	$	—	$	—	$	1,811
Accrued dividends on Preferred Stock	$	1,558	$	1,451	$	7,476
Accretion of fair value of beneficial conversion on preferred stock	$	—	$	—	$	5,313
Accretion of contingent beneficial conversion related on Series C Preferred Stock	$	—	$	—	$	839
Induced conversion of preferred stock in connection with issuance of Series D Preferred Stock	$	—	$	—	$	2,796
Issuance of Common Stock to pay debt	$	—	$	—	$	2,372
Reverse acquisition — net liabilities assumed, excluding cash	$	—	$	—	$	(214	)
Mandatory redeemable convertible preferred stock converted to Common Stock	$	—	$	—	$	500
Common Stock issued to acquire intangible assets	$	—	$	—	$	24
Stock options granted for services	$	—	$	—	$	1,424
Deferred research and development cost resulting from Medtronic Stock Purchase	$	—	$	—	$	795
Acquisition of equipment through capital leases	$	—	$	—	$	106

See accompanying notes to financial statements.

NEUROLOGIX, INC.
(A Development Stage Company)

Notes to Unaudited Financial Statements

(In thousands, except for share and per share amounts)

(1) Description of Business

Neurologix, Inc. (“Neurologix” or the “Company”), is engaged in the research and development of proprietary treatments for disorders of the brain and central nervous system primarily utilizing gene therapies. These treatments are designed as alternatives to conventional surgical and pharmacological treatments. The Company has not generated any operating revenues and, accordingly, it is considered to be a development stage company as defined by Accounting Standards Codification (the “Codification” or “ASC”) Topic 915.

The Company incurred net losses of $7,969, $7,137 and $55,732 and negative cash flows from operating activities of $4,997, $4,013 and $41,576 for the six months ended June 30, 2010 and 2009 and for the period from February 12, 1999 (inception) to June 30, 2010, respectively. The Company expects that it will continue to incur net losses and cash flow deficiencies from operating activities for the foreseeable future.

The Company had cash and cash equivalents of $4,512 and $9,637 as of June 30, 2010 and December 31, 2009, respectively. Based on its cash flow projections, the Company will need additional financing to carry out its planned business activities and complete its plan of operations through December 31, 2010. At the Company’s present level of activities, the Company’s cash and cash equivalents are believed, at this time, to be sufficient to fund its operations only into the fourth quarter of this current fiscal year. Accordingly, there is substantial doubt as to the Company’s ability to continue as a going concern by the end of its current fiscal year.

The Company’s independent registered public accounting firm expressed substantial doubt about the Company’s ability to continue as a going concern in the audit report on the Company’s audited financial statements for the fiscal year ended December 31, 2009 included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2009 (the “2009 10-K”) filed with the Securities and Exchange Commission (the “SEC”) on March 26, 2010.

The Company is currently seeking to raise funds, through public or private equity offerings or debt financings, sufficient to finance its ongoing operations. The Company does not know whether additional financing will be available when needed or, if available, will be on acceptable or favorable terms to it or its stockholders. The financial statements do not include any adjustments that may result from the outcome of this uncertainty.

(2) Basis of Presentation

The accompanying unaudited financial statements of the Company should be read in conjunction with the audited financial statements and notes thereto included in the 2009 10-K. The accompanying financial statements have been prepared in accordance with accounting principles generally accepted in the United States (“GAAP”) for interim financial information, the instructions to Form 10-Q and the rules and regulations of the SEC. Accordingly, since they are interim statements, the accompanying financial statements do not include all of the information and notes required by GAAP for annual financial statements, but reflect all adjustments consisting of normal, recurring adjustments, that are necessary for a fair presentation of the financial position, results of operations and cash flows for the interim periods presented. Interim results are not necessarily indicative of results for a full year. The December 31, 2009 balance sheet information was derived from the audited financial statements as of that date.

(3) Summary of Significant Accounting Policies

(a) Stock-Based Compensation:

At June 30, 2010, the Company had one active share-based employee compensation plan available for grants to employees, non-employee directors and consultants. Stock option awards granted from this plan are granted at the fair market value on the date of grant, vest over a period determined at the time the options are granted, ranging from zero to three years, and generally have a maximum term of ten years. Certain options provide for accelerated vesting if there is a change in control (as defined in the plan) or if there is a termination of employment event for specified reasons set forth in certain employment agreements. When options are exercised, new shares of the Company’s common stock, par value $0.001 per share (the “Common Stock”), are issued.

The Company follows the provisions of ASC Topic 718, “Compensation — Stock Compensation” (“ASC Topic 718”) for employee stock options and other share-based compensation using the modified prospective method. The Company reflects share-based employee compensation cost in net loss.

The total value of the employee stock option awards is expensed ratably over the service period of the employees receiving the awards. As of June 30, 2010, total unrecognized compensation cost related to stock option awards, to be recognized as expense subsequent to June 30, 2010, was approximately $303, and the related weighted-average period over which it is expected to be recognized was approximately 1 year.

The amount of compensation expense recognized during the three and six months ended June 30, 2010 and 2009 was comprised of the following:


	Six Months Ended June 30,						Three Months Ended June 30,
	2010			2009			2010			2009
Research and development	$	100		$	90		$	78		$	72
General and administrative		267			215			118			160

Employee share-based compensation expense	$	367		$	305		$	196		$	232

Net share-based compensation expenses per basic and diluted common share	$	(0.01	)	$	(0.01	)	$	(0.01	)	$	(0.01	)

A summary of option activity as of June 30, 2010 and changes during the six months then ended is presented below:


						Weighted-
	Shares			Weighted-		Average
	Subject to			Average		Remaining		Aggregate
	Option			Exercise		Contractual		Intrinsic
Options	(000)			Price		Term (years)		Value
Outstanding at December 31, 2009		4,174		$	1.19		6.30
Granted		1,015		$	0.65
Exercised		—			—
Forfeited or expired		(582	)		2.29

Outstanding at June 30, 2010		4,607		$	0.93		5.22	$	1,458

Exercisable at June 30, 2010		3,667		$	1.00		4.93	$	1,149

The weighted-average grant-date fair value of options granted during the six months ended June 30, 2010 and 2009 was $0.57 and $0.52, respectively, and was estimated using the Black-Scholes option pricing model.

The following table sets forth the assumptions used with the Black-Scholes option pricing model in determining stock-based compensation under ASC Topic 718 in 2010 and 2009:


	Three and Six Months Ended June 30,
	2010			2009
Expected option term		5-6			5-6
Risk-free interest rate		2.26	%		2.06	%
Expected volatility		129	%		116	%
Dividend yield		0	%		0	%

Expected volatility is based on historical volatility of the Common Stock. The risk-free interest rate is based on the U.S. Treasury security rate.

The expected option term represents the period that stock-based awards are expected to be outstanding based on the simplified method provided in Staff Accounting Bulletin No. 107 (“SAB 107”) which averages an award’s weighted-average vesting period and expected term for “plain vanilla” share options. Under SAB 107, options are considered to be “plain vanilla” if they have the following basic characteristics: granted “at-the-money”; exercisability is conditioned upon service through the vesting date; termination of service prior to vesting results in forfeiture; limited exercise period following termination of service; and options are non-transferable and non-hedgeable.

In December 2007, the SEC issued Staff Accounting Bulletin No. 110 (“SAB 110”). SAB 110 was effective January 1, 2008 and expresses the views of the staff of the SEC with respect to extending the use of the simplified method, as provided in SAB 107, in developing an estimate of the expected term of “plain vanilla” share options in accordance with ASC Topic 718. The Company will continue to use the simplified method until it has the historical data necessary to provide a reasonable estimate of expected life in accordance with SAB 107, as amended by SAB 110. For the expected option term, the Company has “plain-vanilla” stock options and, therefore, used a simple average of the vesting period and the contractual term for options granted subsequent to January 1, 2006 as permitted by SAB 107.

For equity awards to non-employees, the Company also applies the Black-Scholes option pricing model to determine the fair value of such awards in accordance with ASC Topic 718 and the provisions of ASC Topic 505-50, “Equity-Based Payments to Non-Employees.” The options granted to non-employees are re-measured as they vest and the resulting value is recognized as an adjustment against the Company’s net loss over the period during which the services are received.

(b) Basic and Diluted Net Loss Per Common Share:

Basic net loss per common share excludes the effects of potentially dilutive securities and is computed by dividing net loss applicable to common stock by the weighted average number of common shares outstanding for the period. Diluted net income or loss per common share is adjusted for the effects of convertible securities, options, warrants and other potentially dilutive financial instruments only in the periods in which such effects would have been dilutive.

The following securities were not included in the computation of diluted net loss per share because to do so would have had an anti-dilutive effect for the periods presented:


	Six Months Ended June 30,
	2010		2009
Stock options		4,606,833		4,673,833
Warrants		6,535,062		7,441,920
Common Stock issuable upon conversion of Series A Convertible Preferred Stock		645		645
Common Stock issuable upon conversion of Series C Convertible Preferred Stock		6,152,628		6,152,628	¹
Common Stock issuable upon conversion of Series D Convertible Preferred Stock		22,173,636		22,173,636	¹


(1)		These amounts are different from those reported in the Company’s Quarterly Report on Form 10-Q for the period ended June 30, 2009 because the prior number assumed that the Company would pay dividends owed to the holders of Series C Convertible Preferred Stock and Series D Convertible Preferred Stock on conversion of such shares with shares of Common Stock. The current number assumes that such payment will be made with cash.

(c) Derivative Instruments:

The Company’s derivative liabilities are related to warrants issued in connection with financing transactions and are therefore not designated as hedging instruments. All derivatives are recorded on the Company’s balance sheet at fair value in accordance with current accounting guidelines for such complex financial instruments. (See Note 4 and Note 5).

(d) Financial Instruments and Fair Value:

Effective January 1, 2008, the Company adopted provisions of ASC Topic 820, “Fair Value Measurements and Disclosures,” as they relate to financial assets and financial liabilities (“ASC Topic 820”). ASC Topic 820 establishes a fair value hierarchy that prioritizes the inputs to valuation techniques used to measure fair value. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (Level 1 measurements) and the lowest priority to unobservable inputs (Level 3 measurements). The three levels of the fair value hierarchy under ASC Topic 820 are described below:

Level 1 — Unadjusted quoted prices in active markets that are accessible at the measurement date for identical, unrestricted assets or liabilities;

Level 2 — Quoted prices in markets that are not active or financial instruments for which all significant inputs are observable, either directly or indirectly; and

Level 3 — Prices or valuations that require inputs that are both significant to the fair value measurement and unobservable.

In estimating the fair value of the Company’s derivative liabilities, the Company used a probability-weighted Black-Scholes option pricing model. (See Note 4 and Note 5).

Financial assets with carrying values approximating fair value include cash and cash equivalents. Financial liabilities with carrying values approximating fair value include accounts payable and other accrued liabilities.

(e) Recent Accounting Pronouncements:

In January 2010, the Financial Accounting Standards Board issued Accounting Standards Update (“ASU”) 2010-06, “Fair Value Measurements and Disclosures (Topic 820): Improving Disclosures about Fair Value Measurements” (“ASU 2010-06”). ASU 2010-06 includes new disclosure requirements related to fair value measurements, including transfers in and out of Levels 1 and 2 and information about purchases, sales, issuances and settlements for Level 3 fair value measurements. This update also clarifies existing disclosure requirements relating to levels of disaggregation and disclosures of inputs and valuation techniques. The provisions of ASU 2010-06 are effective for periods beginning after December 15, 2009. The disclosures relating to Level 3 activity are effective for fiscal years beginning after December 15, 2010 and for interim periods within those fiscal years. The adoption of ASU 2010-06 did not have a material impact on the Company’s financial statements.

(4) Derivative Financial Instruments

Effective January 1, 2009, the Company adopted the provisions of ASC Topic 815-40, “Derivatives and Hedging: Contracts in Entity’s Own Equity” (“ASC Topic 815-40”). ASC Topic 815-40 clarifies the determination of whether an instrument issued by an entity (or an embedded feature in the instrument) is indexed to an entity’s own stock, which would qualify as a scope exception.

Based upon the Company’s analysis of the criteria contained in ASC Topic 815-40, all warrants (the “Warrants”) issued in connection with the issuance of the Series C Convertible Preferred Stock, par value $0.10 per share, and the Series D Convertible Preferred Stock, par value $0.10 per share must now be treated as derivative liabilities on the Company’s balance sheet.

Consistent with ASC Topic 815-40 requirements, the Company recognized the cumulative effect of the change in accounting principle to reduce the opening balance of the deficit accumulated during the development stage for fiscal year 2009. The cumulative effect adjustment of $5,183 represents the difference between the amounts recognized on the balance sheet before initial application of ASC Topic 815-40 on January 1, 2009. Additionally, the initial fair value of the Warrants, aggregating $6,252, which was initially recorded as additional paid-in capital upon issuance, was reclassified to long-term liabilities upon the adoption of ASC Topic 815-40. The amounts recognized at initial issuance were determined based on the estimated fair value of the Warrants using a probability-weighted Black-Scholes option pricing model. Prospectively, the Warrants will be re-measured at each balance sheet date based on estimated fair value, and any resultant changes in fair value will be recorded as non-cash valuation adjustments within other income (expense) in the Company’s statement of operations.

The Company recorded other expense relating to the change in fair value of the Warrants of $2,588 and $1,980 for the six months ended June 30, 2010 and 2009, respectively. The Company recorded other expense of $2,232 for the three months ended June 30, 2010 and other income of $809 for the three months ended June 30, 2009 relating to the change in fair value of the Warrants. The Company recorded an adjustment in the current period as a result of an over-accrual to the fair value of the Warrants from prior periods. The adjustment was made in the current period as the Company deemed the amounts to be immaterial to the prior periods’ financial statements.

The Company estimates the fair value of the Warrants using a probability-weighted Black-Scholes option pricing model. The assumptions used for the three and six months ended June 30, 2010 and 2009 are noted in the following table:


	Three and Six Months Ended June 30,
	2010	2009
Expected option term	2.9 to 4.4 years	5 to 7 years
Risk-free interest rate	1.79% – 3.28%	2.54% – 3.19%
Expected volatility	129% – 130%	122%
Dividend yield	0%	0%

Expected volatility is based on historical volatility of the Common Stock. The Warrants have a transferability provision and based on guidance provided in SAB 107 for options issued with such a provision, the Company used the full contractual term as the expected term of the Warrants. The risk free interest rate is based on the U.S. Treasury security rates.

(5) Fair Value Measurements

The following tables present the Company’s liabilities that are measured and recognized at fair value on a recurring basis classified under the appropriate level of the fair value hierarchy as of June 30, 2010 and December 31, 2009:

Quoted Prices

in Active

Markets for

Significant

Identical

Other

Significant

Assets and

Observable

Unobservable

Liabilities

Inputs

Balance as of

Description

(Level 1)

(Level 2)

(Level 3)

June 30, 2010

Derivative liabilities related to Warrants

—

6,435

Quoted Prices

in Active

Markets for

Significant

Identical

Other

Significant

Assets and

Observable

Unobservable

Balance as of

Liabilities

Inputs

December

Description

(Level 1)

(Level 2)

(Level 3)

31, 2009

Derivative liabilities related to Warrants

—

3,847

The following tables set forth a summary of changes in the fair value of the Company’s Level 3 liabilities for the six months ended June 30, 2010 and for the year ended December 31, 2009:


	Balance at
	December 31,				Balance as of
Description	2009		Losses		June 30, 2010
Derivative liabilities related to Warrants	$	3,847	$	2,588	$	6,435

Cumulative

Effect of the

Balance at

Adoption of ASC

Balance at

December 31,

Topic 815-40

December

Description

2008

(See Note 4)

Losses

31, 2009

Derivative liabilities related to Warrants

—

1,070

2,777

3,847

The losses on the derivative liabilities are classified in other expenses as a change in derivative liabilities in the Company’s statement of operations. Fair value is determined based on a probability-weighted Black-Scholes option pricing model calculation. (See Note 4).

A financial instrument’s level within the fair value hierarchy is based on the lowest level of any input that is significant to the fair value measurement. At each reporting period, the Company performs a detailed analysis of the assets and liabilities that are subject to ASC Topic 820. At each reporting period, all assets and liabilities for which the fair value measurement is based on significant unobservable inputs or instruments which trade infrequently and therefore have little or no price transparency are classified as Level 3.

(6) Commitments and Contingencies

(a) Consulting Agreements:

On April 26, 2010, the Company and Dr. Michael Kaplitt, one of the Company’s scientific co-founders and a member of its Scientific Advisory Board (the “SAB”), executed a letter agreement that extended the Company’s consulting agreement with Dr. Michael Kaplitt from April 30, 2010 until April 30, 2011 at the annual rate of $175. Related to this agreement, the Company granted Dr. Michael Kaplitt non-qualified stock options to purchase 160,000 shares of Common Stock at an exercise price of $0.65 per share on May 11, 2010. The fair value of the options will be recognized over the period during which the services are received. The amount charged to operations related to these options during the three and six months ended June 30, 2010 was $46.

Effective October 1, 2009, the Company extended, for a period of one year, the term of its consulting agreement with Dr. Matthew During, one of the Company’s scientific co-founders and a member of the SAB. In connection with such extension, the Company granted Dr. Matthew During non-qualified stock options to purchase 60,000 shares of Common Stock at an exercise price of $0.65 per share on May 11, 2010. The fair value of the options will be recognized over the period during which the services are received. The amount charged to operations related to these options during the three and six months ended June 30, 2010 was $20.

(b) Threatened Litigation:

A participant in the Phase 2 clinical trial for Parkinson’s disease, through his counsel, is claiming that he was injured during the trial’s surgical procedure by receiving a double dose of the drug used in the trial on one side of his brain rather than a bilateral dose of such drug as called for by the trial’s protocol. The participant’s counsel, by letter dated June 18, 2010, notified certain parties involved in the trial, including the Company, of his client’s assertion of injury and other claims regarding the conduct of the clinical trial, and requested a settlement of the matter prior to any litigation. The participant’s claimed injury does not represent a serious adverse event, as determined by the monitoring entities that make such determinations, reportable as such to the U.S. Food and Drug Administration (the “FDA”). The Company has reviewed the matter with its counsel and certain of the parties participating in the trial and has discussed the matter with the participant’s counsel. The Company does not believe that the participant’s claimed injury is related to the drug used in the trial or to the trial’s protocol. The Company believes that the participant’s claim against the Company is without merit and, if filed, the Company intends to vigorously defend against such claim.


Item 2.		Management’s Discussion and Analysis of Financial Condition and Results of Operations

The following discussion should be read in conjunction with the unaudited financial statements and accompanying notes in this quarterly report on Form 10-Q and the audited financial statements and notes thereto as of and for the year ended December 31, 2009 included in the 2009 10-K. Operating results are not necessarily indicative of results that may occur in future periods. All amounts in this Item 2 are in thousands.

Business Overview

The Company is a development stage company that is engaged in the research and development of proprietary treatments for disorders of the brain and central nervous system using gene transfer and other innovative therapies. These treatments are designed as alternatives to conventional surgical and pharmacological treatments.

To date, the Company has not generated any operating revenues and has incurred annual net losses. From inception through June 30, 2010, the Company had an accumulated deficit of $59,497, and it expects to incur additional losses for the foreseeable future. The Company recognized net losses of $7,969 for the six months ended June 30, 2010, and $7,137 for the six months ended June 30, 2009.

Since its inception, the Company has financed its operations primarily through sales of its equity and debt securities. From inception through June 30, 2010, the Company received proceeds primarily from private sales of equity and debt securities and from its merger in February 2004 of approximately $44,531 in the aggregate. The Company will continue to seek additional funds through the sale of its securities to fund its operations. (See “Liquidity and Capital Resources”).

The Company has devoted a significant portion of its capital resources to the research and development of its products. The Company’s primary efforts are directed to the development of a therapeutic product to meet the needs of patients suffering from Parkinson’s disease.

In addition to its product for Parkinson’s disease, the Company has undertaken efforts to develop a product for the treatment of temporal lobe epilepsy (“TLE”) but does not anticipate using its current funds for the further development of its TLE product at this time. The Company also has undertaken efforts to develop a product for Huntington’s disease and is engaged in pre-clinical activities relating to such product. See “Plan of Operation — Epilepsy” and “Plan of Operation — Huntington’s Disease” below.

Plan of Operation

Parkinson’s Disease

In June 2010, the Company announced positive results in its Phase 2 clinical trial of its investigational gene therapy for advanced Parkinson’s disease, NLX-P101. This trial was designed to evaluate the safety and efficacy of NLX-P101 in patients with moderate to advanced Parkinson’s disease who were not well-controlled on available medical therapy. Approximately half of the trial participants were randomly selected to receive an infusion of the gene-based treatment bilaterally and the other half, the “Control Participants,” were randomly selected to receive a sterile saline solution.

Trial participants who received NLX-P101 experienced statistically significant and clinically meaningful improvements in off-medication motor scores compared to Control Participants who received sham surgery, measured on the Unified Parkinson’s Disease Rating Scale Part 3 (Motor section). The results also demonstrated a positive safety profile for NLX-P101, with no serious adverse events related to the gene therapy or surgical procedure reported. All treated subjects will continue to be monitored for safety for a 12-month period following their surgical procedure. Control Participants who continue to meet all entry, medical and surgical criteria for the trial will be offered the opportunity to participate in the open label arm of the trial to receive a bilateral infusion of the gene-based treatment.

The Company is currently taking steps to move toward a pivotal trial for treatment of Parkinson’s disease and hopes to be in a position to file its protocol with the FDA in 2011. The ability of the Company to conduct such a trial will require, among other things, the approval of the FDA and the availability of adequate funds. Currently, the Company estimates that the pivotal trial could be completed in 2013 and the estimated total direct costs to reach that milestone are expected to be between $20 million and $40 million.

Epilepsy

In December 2006, the Company submitted an investigational new drug application to the FDA for permission to begin a Phase 1 clinical trial of gene transfer therapy for TLE. The proposed clinical protocol for this study was presented to the National Institute of Health’s Office of Biotechnology Activities Recombinant DNA Advisory Committee on September 23, 2004 and was reviewed favorably.

The Company does not, at this time, intend to commit its current funds to continue work on its gene transfer therapy for TLE. As previously stated, the Company intends to focus its efforts and resources on its Parkinson’s product.

Huntington’s Disease

In November 2005, the Company announced findings from pre-clinical studies that showed that a form of the gene dXIAP may prevent the progression of Huntington’s disease.

The Company’s development of this therapy for Huntington’s disease is currently in the pre-clinical phase. The Company reviewed and analyzed its initial pre-clinical results and determined that additional pre-clinical testing is required prior to seeking regulatory clearance to commence a Phase 1 clinical trial for this therapy.

Other Therapies

The Company will also continue its efforts in developing therapies to treat other neurodegenerative and metabolic disorders, including depression and genetically-based obesity under its research agreements with Cornell University for and on behalf of its Joan & Sanford I. Weill Medical College and Ohio State University.

Future Operating Expenditures

Over the next 12 months, in addition to its normal recurring expenditures, the Company expects to spend approximately $4,600 in Phase 2 clinical trial expenses with regard to its Parkinson’s treatment; $1,200 in expenses in order to scale up its manufacturing capabilities for the supply of product for a Parkinson’s pivotal trial; $1,000 in costs associated with operating as a publicly traded company, such as legal fees, accounting fees, insurance premiums, investor and public relations fees; and $600 in research and licensing fees.

Results of Operations

Three Months Ended June 30, 2010 Compared to the Three Months Ended June 30, 2009

Revenues. The Company did not generate any operating revenues in the three months ended June 30, 2010 or in the three months ended June 30, 2009.

Costs and Expenses.

Research and Development. Research and development expenses decreased by $707 during the three months ended June 30, 2010 to $1,542 as compared to $2,249 during the comparable period in 2009. The decrease was mainly due to a $523 decrease in expenses related to the Company’s Phase 2 clinical trial for Parkinson’s disease, as well as a $124 decrease in costs related to its Huntington’s disease product, an $87 decrease in process development expenses for large scale manufacturing of the Company’s products and infusion devices. These decreases were offset, in part, by increases in miscellaneous research and development expenses.

General and Administrative. General and administrative expenses decreased by $100 to $699 during the three months ended June 30, 2010, as compared to $799 during the comparable period in 2009. This decrease was due mainly to a $77 decrease in cash and non-cash employee compensation expense, as well as a $29 decrease in professional fees, including legal fees, investor relations fees and public relations fees. These decreases were offset, in part, by increases in miscellaneous general and administrative expenses.

Other (Expense) Income, Net. The Company had net other expense of $2,231 during the three months ended June 30, 2010, as compared to net other income of $825 during the comparable period in 2009. The change is mainly due to a $3,041 increase in other expense recognized for the increase in estimated fair value of its derivative liabilities during the three months ended June 30, 2010. The Company recorded an adjustment in the current period as a result of an over-accrual to the fair value of the Warrants from prior periods. The adjustment was made in the current period as the Company deemed the amounts to be immaterial to the prior periods’ financial statements.

Six Months Ended June 30, 2010 Compared to the Six Months Ended June 30, 2009

Revenues. The Company did not generate any operating revenues in the six months ended June 30, 2010 or in the six months ended June 30, 2009.

Costs and Expenses.

Research and Development. Research and development expenses decreased by $259 during the six months ended June 30, 2010 to $3,399 as compared to $3,658 during the comparable period in 2009. The decrease was due, in part, to a $156 decrease in pre-clinical costs associated with the Company’s Huntington’s disease product, as well as a $153 decrease in fees related to license agreements and sponsored research agreements, and a $98 decrease in process development expenses for large scale manufacturing of the Company’s products and infusion devices. These decreases were offset principally by a $147 increase in expenses related to the Company’s Phase 2 clinical trial for Parkinson’s disease.

General and Administrative. General and administrative expenses increased by $435 to $1,983 during the six months ended June 30, 2010, as compared to $1,548 during the comparable period in 2009. This increase was primarily due to an increase in employee compensation expense mainly related to a $98 charge for the accelerated vesting of and the extension of the exercise period for John Mordock’s stock options in connection with his resignation and a $291 charge for severance paid to Mr. Mordock in connection with his resignation. The increase was also due to a $60 increase in professional fees, including legal fees, accounting fees, investor and public relations fees. These increases were offset, in part, by decreases in miscellaneous general and administrative expenses.

Other (Expense) Income, Net. The Company had net other expense of $2,587 during the six months ended June 30, 2010, as compared to net other expense of $1,931 during the comparable period in 2009. The change is mainly due to a $608 increase in other expense recognized for the increase in estimated fair value of its derivative liabilities during the six months ended June 30, 2010. The Company recorded an adjustment in the current period as a result of an over-accrual to the fair value of the Warrants from prior periods. The adjustment was made in the current period as the Company deemed the amounts to be immaterial to the prior periods’ financial statements.

Liquidity and Capital Resources

Cash and cash equivalents were $4,512 at June 30, 2010.

The Company is a development stage company and has not generated any operating revenues as of June 30, 2010. In addition, the Company will continue to incur net losses and cash flow deficiencies from operating activities for the foreseeable future.

Based on its cash flow projections, the Company will need additional financing to carry out its planned business activities and complete its plan of operations through December 31, 2010. At the Company’s present level of activities, the Company’s cash and cash equivalents are believed, at this time, to be sufficient to fund its operations only into the fourth quarter of this current fiscal year. Accordingly, there is substantial doubt as to the Company’s ability to continue as a going concern by the end of its current fiscal year.

In June 2010, the Company announced positive results in its Phase 2 clinical trial of its investigational gene therapy for advanced Parkinson’s disease, NLX-P101. Given these results, the Company is seeking to raise additional funds to develop further its Parkinson’s product as well as to develop its other technologies for the treatment of certain neurological and psychiatric diseases. In this regard, the Company may seek to raise funds through corporate collaborations or licensing arrangements for its Parkinson’s product or other technologies. In addition, the Company is pursuing other strategic transactions which are intended to maximize value for the Company and its stockholders. The Company does not know whether additional financing will be available when needed or, if available, will be on acceptable or favorable terms to it or its stockholders or whether a strategic transaction can be consummated in furtherance of its objectives.

Net cash used in operating activities was $4,997 for the six months ended June 30, 2010 as compared to $4,013 during the comparable period in 2009. The $984 increase in net cash used in operations was primarily due to a $832 increase in net loss for the six months ended June 30, 2010, as well as a $782 increase in cash used as a result of changes to working capital in the first six months of 2010, offset by a $630 increase in non-cash expenses in the first six months of 2010.

The Company had net cash used in investing activities of $128 during the six months ended June 30, 2010 as compared to $157 during the six months ended June 30, 2009. Cash used in investing activities relates to additions to intangible assets and purchases of equipment made by the Company during the first six months of each of 2010 and 2009.

The Company had no net cash used in or provided by financing activities during the six months ended June 30, 2010 and 2009.

FORWARD-LOOKING STATEMENTS

This document includes certain statements of the Company that may constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”) and which are made pursuant to the Private Securities Litigation Reform Act of 1995. These forward-looking statements and other information relating to the Company are based upon the beliefs of management and assumptions made by and information currently available to the Company. Forward-looking statements include statements concerning plans, objectives, goals, strategies, future events, or performance, as well as underlying assumptions and statements that are other than statements of historical fact. When used in this document, the words “expects,” “anticipates,” “estimates,” “plans,” “intends,” “projects,” “predicts,” “believes,” “may,” “should,” “potential,” “continue” and similar expressions, are intended to identify forward-looking statements. These statements reflect the current view of the Company’s management with respect to future events and are subject to numerous risks, uncertainties and assumptions. Many factors could cause the actual results, performance or achievements of the Company to be materially different from any future results, performance or achievements that may be expressed or implied by such forward-looking statements, including, among other things:

•

the inability of the Company to raise additional funds, when needed, through public or private equity offerings, debt financings or additional corporate collaboration and licensing arrangements; and

•

the inability of the Company to successfully commence and complete all necessary clinical trials for the commercialization of its product to treat Parkinson’s disease.

Other factors and assumptions not identified above could also cause the actual results to differ materially from those set forth in the forward-looking statements. Additional information regarding factors which could cause results to differ materially from management’s expectations is found in the section entitled “Risk Factors” contained in the 2009 10-K. Although the Company believes these assumptions are reasonable, no assurance can be given that they will prove correct. Accordingly, you should not rely upon forward-looking statements as a prediction of actual results. Further, the Company undertakes no obligation to update forward-looking statements after the date they are made or to conform the statements to actual results or changes in the Company’s expectations.


Item 3.		Quantitative and Qualitative Disclosures About Market Risk

Not applicable.


Item 4.		Controls and Procedures

(a) Disclosure Controls and Procedures. The Company maintains disclosure controls and procedures as required under Rule 13a-15(e) and Rule 15d-15(e) promulgated under the Exchange Act, that are designed to ensure that information required to be disclosed in the Company’s Exchange Act reports is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and that such information is accumulated and communicated to the Company’s management, including its Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure.

As of June 30, 2010, the Company’s management carried out an evaluation, under the supervision and with the participation of the Company’s Chief Executive Officer and Chief Financial Officer, of the effectiveness of its disclosure controls and procedures. Based on the foregoing, its Chief Executive Officer and Chief Financial Officer concluded that the Company’s disclosure controls and procedures were effective as of June 30, 2010.

(b) Changes in Internal Control Over Financial Reporting. There were no changes in the Company’s internal control over financial reporting that occurred during the period covered by this report that have materially affected, or are reasonably likely to materially affect, the Company’s internal control over financial reporting.

PART II. OTHER INFORMATION


Item 6.		Exhibits

See Exhibit Index.

Signatures

Pursuant to the requirements of the Securities Exchange Act of 1934, the Company has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.


	NEUROLOGIX, INC.
August 12, 2010	/s/ Clark A. Johnson
	Clark A. Johnson
	President and Chief Executive Officer (as Principal Executive Officer)


August 12, 2010	/s/ Marc L. Panoff
	Marc L. Panoff
	Chief Financial Officer, Secretary and Treasurer (as Principal Accounting Officer/Principal Financial Officer)

EXHIBIT INDEX


Exhibit No.		Exhibit

	10.1	Letter Agreement dated April 26, 2010 between Neurologix, Inc. and Dr. Michael G. Kaplitt (filed as Exhibit 10.1 to the Registrant’s Current Report on Form 8-K, dated April 27, 2010, and incorporated herein by reference).

	31.1	Rule 13a-14(a)/15d-14(a) Certification of President and Chief Executive Officer (as Principal Executive Officer).**

	31.2	Rule 13a-14(a)/15d-14(a) Certification of Chief Financial Officer, Secretary and Treasurer (as Principal Accounting Officer/Principal Financial Officer).**

	32.1	Section 1350 Certification of Chief Executive Officer and Chief Financial Officer, Secretary and Treasurer.**


**		Filed herewith

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