Last reviewed · How we verify

NCT03933488

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAK-994 in Healthy Participants

Completed Phase 1 Last updated 24 June 2020
What this trial tests

Phase 1 trial testing TAK-994 in Healthy Participants in 121 participants. Completed in 29 March 2020.

Timeline
1 May 2019
Primary endpoint
29 March 2020
29 March 2020

Quick facts

Lead sponsorTakeda
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingdouble
Primary purposeother
Enrollment121
Start date1 May 2019
Primary completion29 March 2020
Estimated completion29 March 2020
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Takeda — full company profile →

Who can join

18 and older, any sex, with Healthy Participants. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to assess the safety and tolerability of TAK-994 following single and multiple oral doses in healthy non-Japanese and Japanese adult participants and healthy elderly participants.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Hypocretin (Orexin) Replacement Therapies.
    Seigneur E, de Lecea L. · · 2020 · cited 8× · PMID 38738170 · DOI 10.1016/j.medidd.2020.100070

Verify or expand the search:

Other trials of TAK-994

Trials testing the same drug.

Other recruiting trials for Healthy Participants

Currently open trials in the same condition.

Other Takeda trials

Trials by the same sponsor.

Verify against primary sources

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/NCT03933488.

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