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To Investigate Safety, Tolerability, and Pharmacokinetics of Treatment With BI 660848 Rising Single Doses (From 2 mg to 600 mg) Administered as Oral Drinking Solution (Powder in Bottle).

2014-08-27 03:12:54 | BioPortfolio

Summary

As a transition from preclinical investigations to clinical development in this first-in-human trial, safety, tolerability, and pharmacokinetics of BI 660848 will be assessed in human male volunteers using single rising oral doses in order to provide the basis for a potential ongoing clinical development of BI 660848 in the indication of neuropathic pain.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Conditions

Pain

Intervention

BI 660848, BI 660848, BI 660848, BI 660848, BI 660848, BI 660848, BI 660848, BI 660848, BI 660848, BI 660848, BI 660848, Placebo

Location

1284.1.1 Boehringer Ingelheim Investigational Site
Ingelheim
Germany

Status

Recruiting

Source

Boehringer Ingelheim Pharmaceuticals

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:12:54-0400

Clinical Trials [0 Results]

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PubMed Articles [0 Results]

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Medical and Biotech [MESH] Definitions

None available.

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