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NCT00793000
A Phase 1 Study To Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-04287881 After First Time Administration Of Ascending Single Oral Doses To Healthy Adult Subjects
Phase 1 trial testing PF-04287881 in Respiratory Tract Infections in 80 participants. Completed in 1 December 2009.
1 December 2009
Quick facts
| Lead sponsor | Pfizer |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Enrollment | 80 |
| Start date | 1 November 2008 |
| Primary completion | 1 December 2009 |
| Estimated completion | 1 December 2009 |
| Sites | 1 location across United States |
Drugs / interventions tested
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
- PF-04287881 — full drug profile →
- Placebo
Conditions studied
- Respiratory Tract Infections — all drugs for Respiratory Tract Infections →
Sponsor
Pfizer — full company profile →
Who can join
Adults 18 to 55, any sex, with Respiratory Tract Infections. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Evaluation of safety and tolerability of PF-04287881 after single oral dose.
Time frame: Daily up to discharge, follow-up 7-10 days after dosing
Sponsor's own description
The purpose of this study is to determine the safety, tolerability and pharmacokinetics of PF-04287881 after a single oral dose in healthy adult volunteers.
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 NCT00793000
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Currently open trials in the same condition.
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Other Pfizer 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 NCT00793000 (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 Pfizer
- Last refreshed: 3 May 2011
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/NCT00793000.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing