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Safety and Tolerability of GTX-104 Compared with Oral Nimodipine in Patients with ASAH

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NCT05995405

Sponsored by Grace Therapeutics Inc. (industry) · GRCE — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
100estimated
Sites
22
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-10-20actualWhen the study began enrolling
Primary completionDec 2024estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2024estimatedThe whole study's end, after follow-up
First posted2023-08-16actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-10-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Aneurysmal Subarachnoid Hemorrhage (aSAH)

Interventions

  • Drug: GTX-104
  • Drug: Nimotop 30 MG Oral Capsule

Primary outcome

what the primary-completion date above is the date OF
Incidence (% or proportion) of subjects with at least one episode of clinically significant hypotension with a reasonable possibility that GTX-104/oral nimodipine caused the event, according to the Endpoint Adjudication Committee.
measured 90 days

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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