Full Press Release Details
Announces Submission of Investigational New Drug Application
with U.S. FDA to Initiate a Phase 1/2 Clinical Trial Evaluating Gene Therapy
Candidate OCU400 (AAV-NR2E3) to
Treat Inherited Retinal Degeneration
Modifier gene therapy platform has potential
to treat multiple retinal diseases with one product
MALVERN, Pa., - November 8, 2021 - Ocugen, Inc. (NASDAQ:
OCGN), a biopharmaceutical company focused on discovering, developing, and commercializing gene
therapies to cure blindness diseases and developing a vaccine to fight COVID-19, announced that it has submitted an Investigational
New Drug application (IND) with the U.S. Food and Drug Administration (FDA) to initiate a Phase 1/2 clinical trial of OCU400 (AAV-NR2E3),
a modifier gene therapy candidate for the treatment of retinitis pigmentosa resulting from genetic mutations found in NR2E3 and
"This important milestone brings us one step closer towards
achieving our company's vision of fostering a future where no one feels hopeless in the face of disease," said Dr. Shankar
Musunuri, Chairman of the Board, Chief Executive Officer, and Co-Founder of Ocugen. "Our novel modifier gene therapy platform is
a strong example of our approach to drug development."
Ocugen's modifier gene therapy platform aims to target nuclear
hormone receptors (NHRs) that regulate multiple functions within the retina, giving it the potential to address many different gene mutations
- and, in turn, multiple retinal diseases - with a single product. Traditional gene therapy, which transfers a functional
version of a non-functional gene into target cells, targets only one individual gene mutation at a time.
"The goal with OCU400 (AAV-NR2E3)
is to offer people living with genetic vision conditions - people whose vision is slowly deteriorating and who have
no current treatment options - a reason to hope," commented Arun Upadhyay, PhD, Vice President and Head of Research &
Development at Ocugen. "And we're very pleased to be on this journey with the creator of our modifier gene therapy platform,
Dr. Neena Haider from Harvard Medical School. Collaboration is a mother of innovation, and our work with Dr. Haider is really driving
us to see a whole new potential for care."
The planned Phase 1/2 clinical study will evaluate the safety and
proof-of-concept of OCU400, utilizing unilateral sub-retinal injection (one eye per study subject) in 18 patients, with an extension
for contralateral eye and long-term safety follow up. Ocugen has already successfully completed manufacturing at commercial scale (200L)
to support clinical studies. Ocugen plans to follow the Phase 1/2 trial with a Phase 3 study, upon further review of the data.
Between 2019 and 2020, OCU400 was granted four orphan drug
disease designations from the FDA from treating four different gene mutation-associated retinal degenerative diseases. In 2021, the
European Medicines Agency (EMA) granted Ocugen broad orphan medicinal product designation
for OCU400 for the treatment of both retinitis pigmentosa (RP) and Leber Congenital
amaurosis (LCA), meaning that, if approved, OCU400 by itself could treat these diseases that are rooted in mutations of more than
175 different genes.
Ocugen, Inc. is a biopharmaceutical company focused on discovering,
developing, and commercializing gene therapies to cure blindness diseases and developing a vaccine to save lives from COVID-19. 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. We are co-developing Bharat Biotech's COVAXIN vaccine candidate
for COVID-19 in the U.S. and Canadian markets. For more information, please visit www.ocugen.com.
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 forward-looking statements include information about qualitative assessments of available data, potential benefits, expectations
for clinical trials, and anticipated timing of clinical trial readouts and regulatory submissions, including with respect to our planned
Phase 1/2 trial included in our Investigational New Drug application (IND) to the U.S. Food and Drug Administration (FDA) for OCU400.
This information involves risks and uncertainties that could cause actual results to differ materially from those expressed or implied
by such statements. Risks and uncertainties include, among other things, the uncertainties inherent in research and development, including
the ability to meet anticipated clinical endpoints, commencement and/or completion dates for clinical trials, regulatory submission dates,
regulatory approval dates and/or launch dates, as well as risks associated with preliminary and interim data, including the possibility
of unfavorable new clinical trial data and further analyses of existing clinical trial data; the risk that the results of in-vitro studies
will not be duplicated in human clinical trials; the risk that clinical trial data are subject to differing interpretations and assessments,
including during the peer review/publication process, in the scientific community generally, and by regulatory authorities; whether the
FDA will accept our IND submission for OCU400 without any changes, or if we are required to submit additional information to the FDA
in support of our IND submission, the extent and significance of any such changes; whether developments with respect to the COVID-19
pandemic will affect the regulatory pathway available for vaccines in the United States, Canada or other jurisdictions; market demand
for COVAXIN in the United States or Canada; decisions by the FDA or Health Canada impacting labeling, manufacturing processes,
safety and/or other matters that could affect the availability or commercial potential of COVAXIN in the United States or Canada,
including development of products or therapies by other companies. These and other risks and uncertainties are more fully described in
our periodic filings with the Securities and Exchange Commission (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.
Head, Investor Relations & Communications
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