Actinogen's FDA Meeting Sets Path for Alzheimer’s Therapy Approval
Actinogen Medical Limited Achieves Key Milestone with FDA
Actinogen Medical Limited (ASX: ACW) has made significant progress in the quest for approval of Xanamem (emestedastat) as a treatment for Alzheimer’s disease. Recently, the company held a productive Type C meeting with the US Food & Drug Administration (FDA), which has outlined crucial next steps towards marketing approval.
Essential Agreements from the Type C Meeting
During this meeting, Actinogen and the FDA established a mutual understanding concerning essential requirements for the marketing of Xanamem. The discussions focused on several critical components, including regulatory starting materials necessary for drug substance synthesis and the design of an additional pivotal clinical trial.
Key Discussion Points
Some notable agreements reached include:
- The identification of <regulatory starting materials> for the manufacturing process of Xanamem.
- Design elements surrounding the interim analysis for the ongoing XanaMIA trial.
- A definitive plan for a well-controlled, pivotal Phase 3 trial aimed at supporting the previous XanaMIA pivotal outcomes.
- The structure of a major dose trial using a single 10 mg dose of emestedastat versus a placebo.
- Details on how many participants will be treated with Xanamem, underlining FDA guidance for the safety database.
- The number of ancillary clinical pharmacology trials required will be limited.
- Specific nonclinical studies that will further clarify the metabolism and excretion pathways of Xanamem.
Moving Forward with Confidence
The results of this meeting mark a pivotal moment for Actinogen. With clarity on the regulatory pathway acquired from the FDA, the company is gearing up for a timely submission of its New Drug Application (NDA) in the US, alongside approaches to regulatory bodies across the globe.
Future Regulatory Meetings
Excitingly, another crucial meeting is anticipated with the European Medicines Agency in the near future. This will be followed by discussions with other global regulators, such as the UK's Medicines and Healthcare products Regulatory Agency (MHRA), signaling a concerted effort to introduce safer and more effective therapies for Alzheimer’s disease considering the limited effectiveness of existing options.
Actinogen's Commitment to Alzheimer's Treatment
Actinogen's CEO and Managing Director, Dr. Steven Gourlay, expressed enthusiasm about the development, stating the clear guidance from the FDA validates their streamlined development strategy for Xanamem. The agreement on conducting a single pivotal trial signifies a significant step towards securing a marketing application for Alzheimer’s treatment.
About Actinogen Medical Limited
Actinogen Medical is a biotechnology company publicly traded on the ASX under the ticker ACW. The organization is dedicated to innovating therapies to combat Alzheimer’s disease and related conditions. The company is based in Sydney and conducts clinical trials both in Australia and the US.
Xanamem, their prime investigational product, has shown promising results in multiple trials and is designed to exert significant control over cortisol levels in critical regions of the brain. With over 400 individuals already treated, the ongoing XanaMIA trial continues to enroll participants rigorously.
Frequently Asked Questions
What is Xanamem?
Xanamem (emestedastat) is an innovative oral therapy developed by Actinogen Medical for the treatment of Alzheimer’s disease and depression, currently undergoing clinical trials.
What did the FDA agreement entail?
The agreement included a roadmap for regulatory starting materials, the design of a pivotal Phase 3 trial, and the number of participants needed for the safety database.
How does Xanamem work?
Xanamem controls cortisol levels in the brain, which is critical as elevated cortisol is linked to the progression of Alzheimer’s disease.
When is the NDA expected to be submitted?
Actinogen aims for the earliest possible NDA submission following the constructive feedback received from the FDA.
Where can I find more information about Actinogen Medical?
More information about Actinogen Medical and their trials can be accessed through their official channels or upcoming announcements.
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