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Compass Pathways Plc (CMPS)
:CMPS
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COMPASS Pathways (CMPS) Drug Pipeline

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2,128 Followers
Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Psilocybin
Major Depressive Disorder
Phase II
Active Not Recruiting
A Phase II, Multicentre, Randomised, Double-blind, Controlled Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Efficacy of COMP360 in Participants With Recurrent Major Depressive Disorder
Feb 08, 2023
Psilocybin
Treatment Resistant Depression
Phase III
Recruiting
Efficacy, Safety, and Tolerability of Two Administrations of COMP360 in Participants With TRD
Jan 25, 2023
Psilocybin
Treatment Resistant Depression
Phase III
Active Not Recruiting
Efficacy, Safety, and Tolerability of COMP360 in Participants With TRD
Nov 14, 2022
Psilocybin
Anorexia Nervosa
Phase II
Completed
Efficacy and Safety of COMP360 Psilocybin Therapy in Anorexia Nervosa: a Proof-of-concept Study
Jul 28, 2022
Psilocybin
Post Traumatic Stress Disorder
Phase II
Completed
The Safety and Tolerability of COMP360 in Participants With Post-traumatic Stress Disorder
Mar 28, 2022

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases:
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
    What is a clinical trial?
    A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
      What drugs does Compass Pathways Plc (CMPS) have in its pipeline
      CMPS is currently developing the following drugs: Psilocybin, Psilocybin, Psilocybin. These drug candidates are in various stages of clinical development as the company works toward FDA approval.
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