Study Evaluating HTC-867 in Healthy Young and Elderly Subjects
Ascending Single Dose Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HTC-867 Administered Orally to Healthy Subjects
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Terminated
This trial was terminated. No reason was provided.
Other terminated trials from Wyeth is now a wholly owned subsidiary of Pfizer
- Postmenopause · Aug 2010
- Ankylosing Spondylitis · Jul 2010
- Rheumatoid Arthritis · Phase PHASE4 · May 2010
- Fractures · Phase PHASE2/PHASE3 · Mar 2010
- Hemophilia A · Phase PHASE3 · Dec 2009
See all terminations from Wyeth is now a wholly owned subsidiary of Pfizer
Listed as NCT00827489, this PHASE1 trial focuses on Healthy Subjects and remains terminated or withdrawn. Sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, it has been updated 6 times since 2009, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
6 versions recorded-
Sep 2024 — Present [monthly]
Terminated PHASE1
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Jul 2024 — Sep 2024 [monthly]
Terminated PHASE1
-
Jan 2021 — Jul 2024 [monthly]
Terminated PHASE1
-
Jun 2018 — Jan 2021 [monthly]
Terminated PHASE1
-
Feb 2017 — Jun 2018 [monthly]
Terminated PHASE1
▶ Show 1 earlier version
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Jan 2017 — Feb 2017 [monthly]
Terminated PHASE1
First recorded
Jan 2009
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Wyeth is now a wholly owned subsidiary of Pfizer
For direct contact, visit the study record on ClinicalTrials.gov .