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Immunome (IMNM)
NASDAQ:IMNM
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Immunome (IMNM) Drug Pipeline

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343 Followers
Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Varegacestat, Moxifloxacin 400 Mg
Healthy Volunteer
Phase I
Completed
A Cardiac Liability Study of Varegacestat in Healthy Participants
Feb 25, 2025
Varegacestat
Healthy Volunteer
Phase I
Completed
A Phase 1 Mass Balance Study of Varegacestat
Feb 05, 2025
Im-1021
Hematologic Malignancies, Solid Malignancies
Phase I
Recruiting
A Phase 1 Study of IM-1021 in Participants With Advanced Cancer
Feb 04, 2025
Varegacestat
Healthy Volunteer, Hepatic Impairment (Hi)
Phase I
Active Not Recruiting
A Varegacestat Hepatic Impairment Study
Jan 24, 2025
Varegacestat, Itraconazole (200 Mg)
Healthy Volunteer
Phase I
Completed
A Phase 1 Study to Examine the Effects of Itraconazole After Single Dose Administration of Varegacestat (AL102) to Healthy Participants
Nov 04, 2024
Al102
Desmoid, Desmoid Tumor
Phase II/III
Active Not Recruiting
A Study of AL102 in Patients With Progressing Desmoid Tumors
Apr 23, 2021

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 Immunome (IMNM) have in its pipeline
      IMNM is currently developing the following drugs: Varegacestat, Moxifloxacin 400 Mg, Varegacestat, Im-1021. These drug candidates are in various stages of clinical development as the company works toward FDA approval.
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