Clinical trial
A Single-Dose, Open-Label, Parallel Group Study To Evaluate The Pharmacokinetics And Safety Profile Of PROELLEX® (CDB-4124) In Female Subjects With Various Stages Of Impaired Renal Function And In Healthy Female Volunteers
NCT00787618 is registered in ClinicalTrials.gov with Repros Therapeutics Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Single-Dose, Open-Label, Parallel Group Study To Evaluate The Pharmacokinetics And Safety Profile Of PROELLEX® (CDB-4124) In Female Subjects With Various Stages Of Impaired Renal Function And In Healthy Female Volunteers
- Lead sponsor
- Repros Therapeutics Inc.
- Phase
- Phase 1/2
- Overall status
- Terminated
- Start date
- October 31, 2008
- Completion date
- July 31, 2009
- Enrollment
- 6 (actual)
- Sites
- 4
Conditions
As the registry lists them; a condition with its own page is linked.
renal impairment