iECURE Announces FDA Clearance of Investigational New Drug Application for ECUR-506 to Initiate OTC-HOPE Trial for Treatment of Neonatal Onset Ornithine Transcarbamylase Deficiency in the U.S.
- None.
- None.
The FDA's clearance of the IND application for ECUR-506 marks a pivotal step in gene therapy, particularly for rare metabolic liver disorders. From a medical research perspective, the significance of ECUR-506 lies in its potential to offer a therapeutic alternative to liver transplantation, which is currently the primary treatment for neonatal onset OTC deficiency. The use of ARCUS® nuclease for in vivo gene insertion is a novel approach that could pave the way for future gene therapies targeting similar conditions.
Considering the risks associated with liver transplantation, such as the need for lifelong immunosuppression and the possibility of transplant rejection, ECUR-506 could significantly reduce the treatment burden for patients and their families. Additionally, the international scope of the OTC-HOPE study enhances the diversity of the patient population and may expedite the accumulation of data regarding the safety and efficacy of the therapy.
It is also important to note that the success of this trial could have broader implications for the field of gene therapy, potentially encouraging more investment in research and development for treatments of other rare genetic disorders.
From a financial standpoint, the progression of ECUR-506 into clinical trials is a noteworthy development for iECURE, Inc. and its stakeholders. The biotechnology sector is highly sensitive to regulatory milestones and FDA clearance can have a substantial impact on investor confidence and the company's market valuation.
Investors will be closely monitoring the trial's enrollment and subsequent data releases, as positive results could lead to significant value creation. The rarity of OTC deficiency means that ECUR-506 would likely qualify for orphan drug status, potentially resulting in tax credits, grant funding and extended market exclusivity upon approval. These incentives can enhance the financial attractiveness of developing treatments for rare diseases.
However, investors should also be aware of the inherent risks in biotech investing, particularly in early-stage clinical trials. The long development timelines and the possibility of negative or inconclusive results can affect both the stock's volatility and the company's capital requirements.
The healthcare economy is increasingly influenced by advancements in gene therapy and personalized medicine. The development of treatments like ECUR-506 can lead to a paradigm shift in how rare genetic disorders are managed, potentially reducing long-term healthcare costs associated with traditional treatments like organ transplantation.
Additionally, the global collaboration in the OTC-HOPE study reflects a trend towards international partnerships in clinical research, which can be economically beneficial by sharing costs and resources across borders. This approach may also lead to faster market penetration and adoption rates post-approval, as the therapy would already be familiar to a wider range of clinicians and regulatory bodies.
Moreover, success in this area can stimulate more investments in biotech and gene therapy, fostering innovation and economic growth within the sector. It can also encourage policies that support the development of rare disease treatments, which may have positive ripple effects across the healthcare system.
Clinical trial sites in
ECUR-506 is the first in vivo gene insertion program authorized for clinical investigation in infants in the
“With this IND clearance, we are now activating sites in three countries in distinct geographical areas –
The OTC-HOPE study is a Phase 1/2 first-in-human study in newborn males with genetically confirmed neonatal onset OTC deficiency. It is designed primarily to assess the safety and tolerability of ECUR-506 following intravenous administration of a single dose. Secondary objectives are to assess the pharmacokinetics and efficacy of ECUR-506. In addition, exploratory endpoints will assess disease-specific biologic markers, developmental milestones and quality of life. The ECUR-506 program is the first in vivo gene insertion program to be cleared in the
“There is a significant need for clinical research and treatment options for newborns with severe, neonatal onset OTC deficiency,” said Gabriel M. Cohn, MD, Chief Medical Officer of iECURE. “For many families whose children are diagnosed with neonatal onset OTC deficiency, liver transplant is the only curative option, but carries with it serious risks and requires considerable immunosuppressant therapy to prevent transplant rejection. ECUR-506 represents hope for potentially enabling children to produce functional OTC enzyme in the long term without the need for transplantation.”
“This milestone is the culmination of over 8 years of pre-clinical research in my laboratory addressing gene editing strategies for severe rare liver metabolic diseases,” said James M. Wilson, M.D., Ph.D., Rose H. Weiss professor and director, Orphan Disease Center; professor in the Departments of Medicine and Pediatrics, Perelman School of Medicine; and director of the Gene Therapy Program (GTP) at the University of
About ECUR-506
iECURE’s approach to gene editing for its initial programs, including OTC deficiency, relies on the delivery of two adeno-associated virus (AAV) capsids, each carrying different payloads. ECUR-506 comprises two vectors, an ARCUS® nuclease vector targeting gene editing in the well-characterized PCSK9 gene locus and a donor vector that inserts the desired functional OTC gene. iECURE has licensed the ARCUS nuclease for ECUR-506 from Precision BioSciences.1 The cut in the PCSK9 site serves as the insertion site for the OTC gene, providing a potential path to permanent expression of a healthy gene. ECUR-506 is being studied in the OTC-HOPE study, the first clinical meganuclease-based in vivo gene insertion program.
About the OTC-HOPE Study
The OTC-HOPE study is a Phase 1/2 first-in-human clinical trial of ECUR-506 in baby boys with genetically confirmed neonatal onset OTC deficiency and will test differing dose levels of ECUR-506. The study is enrolling baby boys up to seven months who are diagnosed with severe neonatal onset OTC deficiency and meet certain other criteria. The primary objective is to assess the safety and tolerability of intravenous administration of a single dose of ECUR-506. It will also assess the pharmacokinetics and efficacy of ECUR-506 administration and the potential effects of ECUR-506 on disease-specific biologic markers, developmental milestones and quality of life.
About iECURE
iECURE is a clinical-stage gene editing company focused on developing therapies that utilize mutation-agnostic in vivo gene insertion, or knock-in, editing for the treatment of liver disorders with significant unmet need. We believe our approach has the potential to replace and restore the function of a dysfunctional gene, regardless of mutation, by knocking-in a healthy copy of that gene to offer durable gene expression and long-term, potentially curative, therapeutic benefit. Our management team has extensive experience in executing global orphan drug and gene therapy clinical trials and successfully commercializing multiple products. We intend to leverage our team’s core strength in research and development strategy to identify what we believe to be the most suitable target and modality for our product candidates to address particular liver diseases. We are collaborating with the University of Pennsylvania’s Gene Therapy Program (GTP) led by James M. Wilson, M.D., Ph.D., to utilize GTP’s world-class preclinical and translational expertise and infrastructure, which has helped generate our initial pipeline of potential product candidates. For more information, visit https://iecure.com and follow on LinkedIn.
About Precision BioSciences & ARCUS®
Precision BioSciences, Inc. is an advanced gene editing company dedicated to improving life (Nasdaq: DTIL) with its novel and proprietary ARCUS® genome editing platform that is designed to differ from other technologies in the way it cuts, its smaller size, and its simpler structure. Key capabilities and differentiating characteristics may enable ARCUS nucleases to drive more intended, defined therapeutic outcomes. Using ARCUS, Precision’s pipeline is comprised of in vivo gene editing candidates designed to deliver lasting cures for the broadest range of genetic and infectious diseases where no adequate treatments exist. For more information about Precision BioSciences, visit www.precisionbiosciences.com.
Penn’s Financial Disclosure
The University of
[1] iECURE has licensed the ARCUS® nuclease from Precision BioSciences for four gene insertion programs including OTC, CTLN1 and PKU.
View source version on businesswire.com: https://www.businesswire.com/news/home/20240404289854/en/
Investors:
David Garrett
dgarrett@iecure.com
Media:
Janine Bogris
Inizio Evoke Comms
janine.bogris@inizioevoke.com
Source: iECURE, Inc.
FAQ
What is the gene editing therapy being evaluated by iECURE, Inc. for neonatal onset Ornithine Transcarbamylase deficiency in newborn males?
Which countries will be evaluating ECUR-506 for OTC deficiency in newborn males?
What is the primary objective of the OTC-HOPE study by iECURE, Inc.?
Who is the Chief Executive Officer of iECURE, Inc.?
What is the secondary objective of the OTC-HOPE study?
