Clinical trial
Randomized, Double Blind, Placebo Controlled "First-in-human" Study to Assess the Safety and Tolerability of Single Ascending Oral Doses of PBF-1650 (40 mg, 80 mg, 120 and 240 mg) in Healthy Young Male Volunteers.
NCT03798236 is registered in ClinicalTrials.gov with Palobiofarma SL as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Randomized, Double Blind, Placebo Controlled "First-in-human" Study to Assess the Safety and Tolerability of Single Ascending Oral Doses of PBF-1650 (40 mg, 80 mg, 120 and 240 mg) in Healthy Young Male Volunteers.
- Lead sponsor
- Palobiofarma SL
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- December 10, 2018
- Completion date
- May 31, 2019
- Enrollment
- 32 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.