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NCT00833521
A Relative BioAvailability Study of Zolpidem Tartrate 10 mg Tablets Under Fasting Conditions
Phase 1 trial testing Zolpidem 10 mg tablets in Healthy in 38 participants. Completed in 1 February 2002.
1 February 2002
Quick facts
| Lead sponsor | Teva Pharmaceuticals USA |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | other |
| Enrollment | 38 |
| Start date | 1 February 2002 |
| Primary completion | 1 February 2002 |
| Estimated completion | 1 February 2002 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Zolpidem 10 mg tablets — full drug profile →
- AMBIEN® 10 mg tablets — full drug profile →
Conditions studied
- Healthy — all drugs for Healthy →
Sponsor
Teva Pharmaceuticals USA — full company profile →
Who can join
18 and older, any sex, with Healthy. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Cmax - Maximum Observed Concentration
Time frame: Blood samples collected over 24 hour period
Bioequivalence based on Cmax -
AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated)
Time frame: Blood samples collected over 24 hour period
Bioequivalence based on AUC0-inf -
AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant)
Time frame: Blood samples collected over 24 hour period
Bioequivalence based on AUC0-t
Sponsor's own description
The objective of this study is to compare the relative bioavailability of Zolpidem tartrate 10 mg tablets (manufactured by TEVA Pharmaceutical Industries, Ltd. and distributed by TEVA Pharmaceuticals USA) with that of AMBIEN® tablets(G.D. Searle \& Co.) in healthy, adult, non-smoking subjects under fasting conditions.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT00833521
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Teva Pharmaceuticals USA trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00833521 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Teva Pharmaceuticals USA
- Last refreshed: 19 August 2024
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/NCT00833521.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing