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ACER-002

Not yet reviewed: Listed from FDA or ClinicalTrials.gov records; an editor has not checked it yetListed from FDA or ClinicalTrials.gov records; an editor has not checked it yet.

Acer Therapeutics Inc. · Vascular Ehlers-Danlos Syndrome

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Key figures

  • Next catalyst

    None scheduled

    Only dates with a source are listed

  • Phase

    Phase 3

    Not recorded

  • Linked trials

    1

    From ClinicalTrials.gov

  • Latest FDA action

    None on record

    From Drugs@FDA

Recalls, shortages, patents and EU status at a glance

Key information

Sponsor
Acer Therapeutics Inc. Source: Company record for Acer Therapeutics Inc. (opens in a new tab)
Indication
Vascular Ehlers-Danlos Syndrome Source: Conditions from ClinicalTrials.gov (opens in a new tab)
Designations
None recorded
Next catalyst
None scheduled

Development timeline

  1. Preclinical Completed
  2. Phase 1 Completed
  3. Phase 2 Completed
  4. Phase 3 Current stageFirst trial start 7 Nov 20221 linked trial
  5. Filed Not yet
  6. Approved Not yet

The evidence trail loads here.

Overview

Mechanism
Not recorded
Route
Not recorded
Modality
Not recorded
Specialties
Not recorded

Overview text is written by HealthTrade editors.

Key dates

No catalysts yet. Editors add each date together with its source.

FDA designations

No FDA designations are on record for ACER-002. Editors add each one with its source.

Filed application

No filed application is on record for ACER-002. Approvals are listed under FDA actions.

FDA advisory committees

No FDA advisory committee meetings are on record for ACER-002.

Clinical trials

Trials linked to ACER-002
TrialTitlePhaseStatusEnrollmentPrimary completionResults posted
NCT05432466ClinicalTrials.gov record for NCT05432466 (opens in a new tab)DiSCOVERClinical Trial to Compare the Efficacy of Celiprolol to Placebo in Patients With Vascular Ehlers-Danlos SyndromePhase 3Recruiting150 (estimated)1 Mar 2029 (estimated) No

Source: ClinicalTrials.gov, U.S. National Library of Medicine. Posted results are shown as ClinicalTrials.gov prints them; results from company and journal sources are entered by editors and listed separately. Full result tables are on ClinicalTrials.gov.

Trial quality

About CT-VCA

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FDA actions

No FDA approvals on record for this drug.

FDA recalls load here.

FDA drug shortages load here.

Orange Book patents load here.

FAERS adverse event counts load here.

Papers and preprints load here.

Community discussion loads here.

EU status (EMA)

EMA's medicines data lists no human medicine with the same active substance as ACER-002.

Source: European Medicines Agency (EMA), medicines data download.

Related news

No recent headlines mention this drug.

Sources

Record updated .

Dates come from company and FDA disclosures and can change. Nothing on this page is investment advice.