Ensysce Biosciences Inc

Noticias y eventos de Ensysce Biosciences Inc (ENSC)

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Noticias de ENSC

Eventos de ENSC

10/23 17:00

Selling Stockholders Plan to Sell 433.91M Shares of Common Stock

This filing relates to the offer and sale from time to time by the selling stockholders of up to 433.91M shares of common stock. The company is not selling any shares under this prospectus and will not receive any of the proceeds from the sale of shares by the selling stockholders.

9/24 09:00

Ensysce Biosciences Submits Phase 2a Study Protocol for CY200

Ensysce Biosciences announced the submission of the protocol for a Phase 2a clinical study of CY200, the Company's newest drug candidate from the newly acquired Cy Biopharma. This milestone involved the submission of protocol CYBIO_001 entitled "A Phase 2A, Multicenter, Randomised, Double-blind, Placebo-controlled, Parallel-group, Proof of-Concept Study to Evaluate the Efficacy, Safety, and Tolerability of CY200 in Participants with Complex Regional Pain Syndrome Type 1" to the Medicines and Healthcare products Regulatory Agency of the UK where the study will be conducted. CYBIO_001 is designed to evaluate the analgesic efficacy of CY200 compared to placebo in adult participants with CRPS Type 1.

9/14 08:30

Ensysce Biosciences Executive Attends FDA Hearing on Psychedelic Drugs

Ensysce Biosciences announced that Richard Langford, Chief Medical Officer of Cy Biopharma, has been selected to present in person at the U.S. Food and Drug Administration's public hearing, "Considerations for Potential Future Therapeutic Use of Psychedelic Drugs," being held today, Monday, September 14 at the FDA's White Oak Campus in Silver Spring, Maryland. Dr. Langford is among a limited group of stakeholders granted the opportunity to provide comments at the hearing in the afternoon session 'Considerations for access; Best practices for data collection and standardization". Ensysce announced the acquisition of Cy Biopharma on August 6. The FDA is holding the hearing in collaboration with federal partners to obtain feedback and perspectives on issues associated with the potential future therapeutic use of drug products containing a psychedelic drug substance in supervised and supportive settings. The hearing supports implementation of Executive Order 14401, "Accelerating Medical Treatments for Serious Mental Illness," which directs federal agencies to accelerate the research, review and approval of psychedelic drugs for the treatment of serious mental health conditions.

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