OCGN Ocugen Inc

Ocugen Provides Business Update and Full Year 2019 Financial Results

Ocugen Provides Business Update and Full Year 2019 Financial Results

Over 95% planned enrollment completed in Phase 3 oGVHD study; topline results anticipated by end of 2020

Conference Call and Webcast Today at 8:30 a.m. ET

MALVERN, Pa., March 27, 2020 (GLOBE NEWSWIRE) -- Ocugen, Inc. (NASDAQ: OCGN), a clinical-stage company focused on discovering, developing and commercializing transformative therapies to treat rare and underserved ophthalmic diseases, today reported full year 2019 financial results along with a general business update.

“We are extremely pleased with the progress we have made in enrolling patients in our Phase 3 clinical trial for OCU300, an orphan drug candidate for ocular graft versus host disease (oGVHD). Based on current enrollment, we anticipate topline results by the end of the year,” commented Shankar Musunuri, PhD, MBA, Chairman, CEO and Co-Founder of Ocugen. “The publication of preclinical data on OCU400 in Nature Gene Therapy earlier this month is a key achievement for this program. We continue to advance IND-enabling studies toward bringing this potential breakthrough modifier gene therapy platform to patients in a Phase 1/2a clinical trial for OCU400 in 2021. Similar to the situation with virtually all other biopharmaceutical companies, we are also assessing the potential impact of ongoing COVID-19 pandemic-related events on our programs and plans. We are grateful to healthcare professionals and others who are working hard to address and mitigate the challenges presented by the virus.”

Business Highlights:

  • OCU300 (oGVHD) – In December 2019, Ocugen announced 50% enrollment in its Phase 3 trial, and as of March 20, 2020, Ocugen has completed over 95% of the planned enrollment. Ocugen is anticipating topline results by the end of the year.



  • OCU400 (AAV-NR2E3) – On March 3, 2020, Nature Gene Therapy published preclinical data related to OCU400, supporting the use of nuclear hormone receptor gene NR2E3 as a genetic modifier and therapeutic agent to treat multiple retinal degenerative diseases and potentially serve as a broad-spectrum therapy for retinitis pigmentosa.



  • EB-5 Loan Agreement – On March 26, 2020, Ocugen drew down an additional $0.5 million under its loan agreement with EB5 Life Sciences, L.P.

Full Year 2019 Financial Results:

  • Ocugen’s cash, cash equivalents and restricted cash totaled $7.6 million as of December 31, 2019, compared to $1.8 million as of December 31, 2018.



  • Research and development expenses for the year ended December 31, 2019 were $8.1 million compared to $10.3 million for the year ended December 31, 2018. General and administrative expenses for the year ended December 31, 2019 were $6.1 million compared to $5.8 million for the year ended December 31, 2018.



  • Ocugen reported a net loss of $20.2 million, or $1.46 loss per share, for the year ended December 31, 2019, compared to a net loss of $18.2 million, or $3.67 loss per share, for the year ended December 31, 2018.



  • The Company had 52,625,228 shares of common stock outstanding as of December 31, 2019.

Conference Call and Webcast Details

The Company has scheduled a conference call and webcast for 8:30 a.m. ET today to discuss the results and recent business highlights. Ocugen's senior management team will host the call, which will be open to all listeners. There will also be a question and answer session following the prepared remarks.

The call can be accessed by dialing (844) 873-7330 (U.S.) or (602) 563-8473 (international) and providing the conference ID 5373849. To access a live audio webcast of the call on the “Investors” section of the Ocugen website, please click here. A replay of the webcast will be archived on Ocugen’s website for approximately 45 days following the call.

About Ocugen, Inc.

Ocugen, Inc. is a clinical-stage biopharmaceutical company focused on discovering, developing and commercializing transformative therapies to treat the whole eye. Our Phase 3 small molecule drug candidate for ocular Graft Versus Host Disease (oGVHD), if approved, will be the first and only treatment for this orphan disease. Our breakthrough modifier gene therapy platform has the potential to treat multiple retinal diseases with one drug – “one to many”. And our novel biologic product candidate aims to offer better therapy to patients with underserved diseases such as wet age-related macular degeneration, diabetic macular edema and diabetic retinopathy. For more information, please visit

Cautionary Note on Forward-Looking Statements

This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995, which are subject to risks and uncertainties. We may, in some cases, use terms such as “predicts,” “believes,” “potential,” “proposed,” “continue,” “estimates,” “anticipates,” “expects,” “plans,” “intends,” “may,” “could,” “might,” “will,” “should” or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Such statements are subject to numerous important factors, risks and uncertainties that may cause actual events or results to differ materially from our current expectations. These and other risks and uncertainties are more fully described in our periodic filings with the Securities and Exchange Commission (the “SEC”), including the risk factors described in the section entitled “Risk Factors” in the quarterly and annual reports that we file with the SEC. Any forward-looking statements that we make in this press release speak only as of the date of this press release. Except as required by law, we assume no obligation to update forward-looking statements contained in this press release whether as a result of new information, future events or otherwise, after the date of this press release.

(tables to follow)



OCUGEN, INC.

CONSOLIDATED BALANCE SHEETS

(UNAUDITED)

 December 31,

2019
 December 31,

2018
Assets   
Current assets   
Cash and cash equivalents$7,444,052   $1,628,136  
Prepaid expenses and other current assets1,322,167   313,499  
Asset held for sale7,000,000     
Total current assets15,766,219   1,941,635  
Property and equipment, net222,464   245,788  
Restricted cash151,016   150,477  
Other assets667,747   116,333  
Total assets$16,807,446   $2,454,233  
Liabilities and stockholders’ equity (deficit)   
Current liabilities   
Accounts payable$1,895,613   $3,277,525  
Accrued expenses2,270,045   1,402,750  
Short-term debt, net   7,483,847  
Derivative liabilities   1,741,222  
Operating lease obligation172,310     
Other current liabilities205,991   204,242  
Total current liabilities4,543,959   14,109,586  
Non-current liabilities   
Operating lease obligation, less current portion163,198     
Long term debt, net1,072,123   1,016,727  
Other non-current liabilities9,755   37,459  
Total liabilities5,789,035   15,163,772  
Stockholders’ equity (deficit)   
Common stock527,467   49,606  
Treasury stock(47,864)    
Accumulated other comprehensive income   451  
Additional paid-in capital62,018,632   18,477,598  
Accumulated deficit(51,479,824)  (31,237,194) 
Total stockholders’ equity (deficit)11,018,411   (12,709,539) 
Total liabilities and stockholders’ equity (deficit)$16,807,446   $2,454,233  



OCUGEN, INC.

CONSOLIDATED STATEMENTS OF OPERATIONS

(UNAUDITED)

 Year ended December 31,
 2019 2018
Operating expenses:   
Research and development$8,085,522   $10,321,397  
General and administrative6,077,097   5,819,111  
Total operating expenses14,162,619   16,140,508  
Loss from operations(14,162,619)  (16,140,508) 
Other income (expense)   
Change in fair value of derivative liabilities(3,187,380)  1,664,689  
Loss on debt conversion(341,136)    
Interest income1,214   19,213  
Interest expense(1,767,836)  (3,750,630) 
Other income (expense)(784,873)  (12,428) 
Total other income (expense)(6,080,011)  (2,079,156) 
Net loss$(20,242,630)  $(18,219,664) 
    
Net loss per share of common stock—basic and diluted$(1.46)  $(3.67) 
Weighted average common shares outstanding—basic and diluted13,893,819   4,960,552  

 

Corporate Contact:
Ocugen, Inc.
Kelly Beck    

Media Contact:
LaVoieHealthScience
Emmie Twombly
 
 
EN
27/03/2020

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Ocugen Inc

 PRESS RELEASE

Ocugen Announces Early Completion of Dosing in Phase 2/3 Pivotal Confi...

Ocugen Announces Early Completion of Dosing in Phase 2/3 Pivotal Confirmatory Trial of OCU410ST for Stargardt Disease GARDian3 trial enrollment and dosing completed (N=63) in less than nine monthsTopline results expected in 2Q27 with BLA to follow by mid-2027OCU410ST represents a potential first-in-class, one-time modifier gene therapy for all ABCA4-associated retinopathies MALVERN, Pa., April 01, 2026 (GLOBE NEWSWIRE) -- Ocugen, Inc. (Ocugen or the Company) (NASDAQ: OCGN), a pioneering biotechnology leader in gene therapies for blindness diseases, today announced that dosing has been s...

 PRESS RELEASE

Ocugen Announces Topline 12-month Data from Phase 2 ArMaDa Clinical Tr...

Ocugen Announces Topline 12-month Data from Phase 2 ArMaDa Clinical Trial Evaluating OCU410 Modifier Gene Therapy for Geographic Atrophy Secondary to Dry Age-Related Macular Degeneration Optimal dose intended for Phase 3 demonstrates statistically significant reduction in lesion growth (31%) versus control at 12 months (p< 0.05)Potential 2X treatment benefit compared to 15% and 22% reductions reported for currently approved therapies at 12 and 24 months, respectivelyNo serious adverse events and no adverse events of special interest related to OCU410 reported to date MALVERN, Pa., March 2...

 PRESS RELEASE

Ocugen to Host Webcast on Tuesday, March 24 at 8 a.m. EDT to Discuss P...

Ocugen to Host Webcast on Tuesday, March 24 at 8 a.m. EDT to Discuss Phase 2 Clinical Trial Data for OCU410—Modifier Gene Therapy for Geographic Atrophy MALVERN, Pa., March 23, 2026 (GLOBE NEWSWIRE) -- Ocugen, Inc. (“Ocugen” or the “Company”) (NASDAQ: OCGN), a pioneering biotechnology leader in gene therapies for blindness diseases, today announced that it will host a conference call and live webcast with key opinion leaders (KOLs) and Ocugen executive leadership to discuss the full data set from the Phase 2 ArMaDa clinical trial evaluating OCU410 for geographic atrophy (GA), late-stage d...

 PRESS RELEASE

Ocugen Provides Business Update with Fourth Quarter and Full Year 2025...

Ocugen Provides Business Update with Fourth Quarter and Full Year 2025 Financial Results Conference Call and Webcast Today at 8:30 a.m. ET Enrollment for the OCU400 Phase 3 liMeliGhT clinical trial—the first and largest gene therapy registrational trial for broad retinitis pigmentosa patients—was completed. Topline Phase 3 data expected in the first quarter 2027, advancing OCU400 towards potential approval in 2027.OCU410ST Phase 2/3 pivotal confirmatory trial nearing enrollment completion. Interim data expected in the third quarter 2026, followed by topline Phase 2/3 data in the second qu...

 PRESS RELEASE

Ocugen Announces Phase 3 liMeliGhT Enrollment Completion for OCU400, a...

Ocugen Announces Phase 3 liMeliGhT Enrollment Completion for OCU400, a Novel Modifier Gene Therapy for Broad Retinitis Pigmentosa Enrollment for liMeliGhT, the first and largest gene therapy registrational trial for broad retinitis pigmentosa (RP) patients, was completed, reflecting strong interest from investigators and patientsTopline Phase 3 data expected in 1Q 2027, advancing OCU400 towards potential approval in 2027 as a treatment option for early- to late-stage RPPositive long-term, 3-year Phase 1/2 durable, safety and tolerability data for OCU400 demonstrates sustained clinically mea...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch