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NCT05487781

Phase 1 Clinical Study to Describe Biological Safety and Pharmacokinetics of Tyrphostin

Status unknown EARLY_PHASE1 Last updated 4 August 2022
What this trial tests

EARLY_PHASE1 trial testing Tirfostina/L-Carnitina in Healthy in 48 participants. Status unknown.

Timeline
24 May 2022
Primary endpoint
28 June 2022
29 July 2022

Quick facts

Lead sponsorMolecule X LLC
PhaseEARLY_PHASE1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingdouble
Primary purposetreatment
Enrollment48
Start date24 May 2022
Primary completion28 June 2022
Estimated completion29 July 2022
Sites1 location across Mexico

Drugs / interventions tested

Conditions studied

Sponsor

Molecule X LLC

Who can join

Adults 18 to 55, any sex, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluate the biological safety and pharmacokinetics of tyrphostin AG-17 present in the solid oral formulations of the fixed-dose combination, in three different concentrations of the compound tyrphostin AG-17 contained 10 mg, 3.3 mg and 1 mg, respectively, with 700 mg of L-Carnitine tartrate each presentation, in a single dose in healthy research subjects of Mexican nationality.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05487781.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing