TipRanks
Go Ultimate55% OFF

Annexon Biosciences (ANNX) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
TanruprubartGuillain-Barre SyndromePhase IIINot Yet RecruitingAn Open Label Clinical Study to Evaluate Tanruprubart (Also Commonly Known as ANX005) in Participants With Guillain-Barré Syndrome (FORWARD Study)Jun 06, 2025―
Sham Administration, Anx007Geographic AtrophyPhase IIIRecruitingA Study Investigating the Efficacy and Safety of Intravitreal (IVT) Injections of ANX007 in Participants With Geographic Atrophy (GA)Jul 15, 2024―
Anx1502HealthyPhase ICompletedDose Study of ANX1502 in Healthy VolunteersAug 28, 2022―
Anx005Guillain-Barre SyndromePhase IIICompletedEfficacy and Safety of ANX005 in Subjects With Guillain-Barré SyndromeJan 06, 2021―
Anx005Amyotrophic Lateral SclerosisPhase IICompletedStudy of ANX005 in Adults With Amyotrophic Lateral Sclerosis (ALS)Sep 23, 2020―

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 Annexon Biosciences, Inc. (ANNX) have in its pipeline
Annexon Biosciences ANNX is currently developing the following drugs: Tanruprubart, Sham Administration, Anx007, Anx1502, Anx005. These drug candidates are in various stages of clinical development as the company works toward FDA approval.