Full Press Release Details
Ocugen Announces New Cell Therapy Program Following
FDA Regenerative Medicine Advanced Therapy (RMAT) Recognition
(autologous chondrocyte-derived neocartilage) receives regulatory designation intended to help expedite development of new regenerative
MALVERN, Pa. - May 24, 2022
(GLOBE NEWSWIRE) - Ocugen, Inc. (NASDAQ: OCGN), a biotechnology company focused on discovering, developing, and commercializing
novel gene therapies, biologicals, and vaccines, today announced that it is diversifying its innovative pipeline by introducing
a Phase 3, cell therapy platform technology called NeoCart (autologous chondrocyte-derived neocartilage). Recently, the
U.S. Food and Drug Administration (FDA) granted a Regenerative Medicine Advanced Therapy (RMAT) designation to NeoCart
for the repair of full-thickness lesions of the knee cartilage in adults.
NeoCart is a three-dimensional
tissue-engineered disc of new cartilage that is manufactured by growing chondrocytes - the cells responsible for maintaining
cartilage health - derived from the patient on a unique scaffold. NeoCart has the potential to accelerate healing
and reduce pain by rebuilding a patient's damaged knee cartilage. It treats pain at the source, creating a similar, functional joint
surface as it was before the injury. Ultimately, the goal is to prevent a patient's progression to osteoarthritis. NeoCart
was acquired as a part of Ocugen's reverse merger with the original developer of the therapy, Histogenics, in 2019.
"We're excited that NeoCart has received
this RMAT designation, an important regulatory milestone, especially as we view this product as an enabling technology in cell and regenerative
therapy for orthopedic indications. Our next step will be working with the FDA to construct the Phase 3 program to bring this innovation
to this emerging treatment area," said Dr. Shankar Musunuri, Chairman, CEO, and Co-Founder, Ocugen, Inc. "People
living with articular cartilage lesions literally have holes in their knees that are extremely difficult to heal, and without proper treatment,
they're at high risk of getting osteoarthritis. We believe that NeoCart offers the potential for an innovative new
option where treatments in this area are still limited and results are not optimal."
The Regenerative Medicine Advanced Therapy
(RMAT) designation is part of the 21st Century Cures Act. The program was created to expedite the development and review of
regenerative medicine therapies intended to treat, modify, reverse or cure a serious condition. Receiving an RMAT designation offers
sponsor companies all the benefits of the fast track and breakthrough therapy designation programs, including early interactions with
the FDA. Ocugen is working with the FDA to finalize the Phase 3 protocols necessary to advance the clinical development program of NeoCart
required for eventual market authorization.
Articular cartilage lesions are a serious
and often mobility-limiting condition. When the cartilage is healthy, it makes movement easy, allowing the bones to glide over
each other with very little friction, but it can be damaged by injury or normal wear and tear. Cartilage that is damaged can, over time,
cause pain and reduce one's ability to function. Small articular lesions have a limited capacity to self-repair, and full thickness
injuries have no ability to naturally heal. There are no blood vessels or nerves to support healing, and as cartilage matures, chondrocytes
have limited ability to replicate. Untreated damage eventually can lead to osteoarthritis.
Details of the NeoCart
development program will be shared at a future date.
is a biotechnology company focused on discovering, developing, and commercializing novel gene and cell therapies, biologicals and vaccines
that improve health and offer hope for people and global communities. We are making an impact through courageous innovation, taking science
in new directions in service of patients. Our breakthrough modifier gene therapy platform has the potential to treat multiple diseases
with one drug and we are advancing research in other therapeutic areas to offer new options for people with unmet medical needs. Discover
Cautionary Note on Forward-Looking
release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995, which are subject
to risks and uncertainties. Ocugen 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, but are not limited to, statements about Ocugen's intention to work with the U.S. Food and Drug Administration ("FDA")
to finalize the Phase 3 protocols necessary to advance the clinical development program of NeoCart (autologous
chondrocyte-derived neocartilage) required for eventual market authorization. Such statements are
subject to numerous risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such
statements, including, among other things, the uncertainties inherent in research and development, including the ability to meet anticipated
clinical endpoints, ability to timely enroll clinical trial participants, commencement and/or completion dates for clinical trials, regulatory
submission dates, regulatory approval dates and/or launch dates, Ocugen's ability to utilize accelerated FDA review designations,
such as the Regenerative Medicine Advanced Therapy designation, which does not guarantee an accelerated pathway or timeline for regulatory
approval of any such product candidates, including NeoCart (autologous chondrocyte-derived neocartilage), or increase
the likelihood of any such approvals, and the other risks and uncertainties 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.
Head, Investor Relations & Communications
For investor-related inquiries: IR@Ocugen.com