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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.