# Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously

> **NCT00783341** · PHASE1 · COMPLETED · sponsor: **Wyeth is now a wholly owned subsidiary of Pfizer** · enrollment: 25 (actual)

## Conditions studied

- Healthy Subjects

## Interventions

- **DRUG:** GAP-134
- **DRUG:** placebo

## Key facts

- **NCT ID:** NCT00783341
- **Lead sponsor:** Wyeth is now a wholly owned subsidiary of Pfizer
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE1
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2008-11
- **Primary completion:** 2009-02
- **Final completion:** 2009-02
- **Target enrollment:** 25 (ACTUAL)
- **Last updated:** 2009-07-17


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00783341

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00783341, "Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously". Retrieved via AI Analytics 2026-07-20 from https://api.ai-analytics.org/clinical/NCT00783341. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
