A PHASE 1, OPEN-LABEL, SINGLE-DOSE, NON-RANDOMIZED PARALLEL GROUP STUDY TO COMPARE THE PHARMACOKINETICS, SAFETY, AND TOLERABILITY OF OSIVELOTOR (PF-07940367) IN ADULT PARTICIPANTS WITH MILD AND MODERATE HEPATIC IMPAIRMENT
Latest Information Update: 14 Jan 2025
Price :
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At a glance
- Drugs Osivelotor (Primary)
- Indications Renal failure
- Focus Pharmacokinetics
- Sponsors Pfizer
- 10 Jan 2025 Status changed from recruiting to completed.
- 08 Oct 2024 Planned End Date changed from 1 Jun 2025 to 9 Jun 2025.
- 08 Oct 2024 Planned primary completion date changed from 1 Jun 2025 to 9 Jun 2025.