Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05236738 · ClinicalTrials.gov registry record · Phase 1

A Study to Compare the Drug Levels of Atazanavir and Cobicistat Between the Coadministration of Age-Appropriate Mini-Tablet Formulations and the Coadministration of the Individual Reference Products in Healthy Adults Under Fed Conditions

A Phase 1 study of Healthy Participants, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
42
Enrollment target
1
Study location

NCT05236738: Completed Phase 1 study of Healthy Participants, sponsored by Bristol-Myers Squibb.

NCT05236738 is a Phase 1 study of Healthy Participants that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 42 participants, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (35% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05236738, a Phase 1 study of Healthy Participants, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
42 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the drug absorption of atazanavir and cobicistat between the coadministration of the mini-tablet formulations in applesauce or chocolate pudding followed by water and the coadministration of atazanavir oral powder in applesauce and cobicistat oral tablet followed by water in healthy adult participants.

Conditions Studied

Interventions

  • DRUG Cobicistat
  • DRUG Atazanavir
  • DRUG Atazanavir/Cobicistat Mini-tablet

Study Locations (1)

Florida

  • Local Institution - 0001 - Miami

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2022-05-13
Est. Completion 2022-07-26
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT05236738 record still lists

NCT05236738 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (35% lower).

The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 3 interventions - of which Cobicistat is the first listed.

NCT05236738 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT05236738 about?

NCT05236738 is a clinical study titled "A Study to Compare the Drug Levels of Atazanavir and Cobicistat Between the Coadministration of Age-Appropriate Mini-Tablet Formulations and the Coadministration of the Individual Reference Products in Healthy Adults Under Fed Conditions". The purpose of this study is to evaluate the drug absorption of atazanavir and cobicistat between the coadministration of the mini-tablet formulations in applesauce or chocolate pudding followed by water and the coadministration of atazanavir oral powder in applesauce and cobicistat oral tablet foll...

What is the current status of trial NCT05236738?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2022-05-13. Estimated completion is 2022-07-26.

What conditions does trial NCT05236738 study?

This clinical trial studies the following conditions: Healthy Participants.

What interventions are being tested in trial NCT05236738?

The interventions under investigation include: Cobicistat (DRUG), Atazanavir (DRUG), Atazanavir/Cobicistat Mini-tablet (DRUG).

Who is sponsoring clinical trial NCT05236738?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05236738 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Participants

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05236738's enrollment target sits among peer trials

42 55th of 119 higher than 65 of 119 other Healthy Participants trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy Participants trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02852213 · 42 participants · Phase 1

    A Single-Stage, Adaptive, Open-label, Dose Escalation Safety and Efficacy Study of AADC Deficiency in Pediatric Patients

  • NCT03136146 · 42 participants · Phase 2

    Combination Chemotherapy in Treating Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia, Lymphoblastic Lymphoma, Burkitt Lymphoma/Leukemia, or Double-Hit Lymphoma/Leukemia

  • NCT03178149 · 42 participants · Phase 1

    A Study of the Safety and Tolerability of ASP7317 in Senior Adults Who Are Losing Their Clear, Sharp Central Vision Due to Geographic Atrophy Secondary to Dry Age-related Macular Degeneration

  • NCT03663530 · 42 participants · NA

    Circadian Misalignment and Energy Balance

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05236738, the US trial registry maintained by the National Library of Medicine. NCT05236738 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.