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Terminated Phase 2 Interventional Results available

Leidos-Enabled Adaptive Protocol (LEAP-CT) for Evaluation of Post-exposure Prophylaxis for Newly-infected COVID-19 Patients

ClinicalTrials.gov ID: NCT05077969

Public ClinicalTrials.gov record NCT05077969. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 5, 2026, 1:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Virtual Phase 2 Randomized, Placebo-controlled, Double-blind Study to Evaluate the Safety and Efficacy of the Combination of Famotidine and Celecoxib as a Post-exposure Prophylaxis (PEP) for Newly-infected COVID-19 Patients

Study identification

NCT ID
NCT05077969
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Leidos Life Sciences
Industry
Enrollment
4 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 28, 2021
Primary completion
Jun 27, 2022
Completion
Jul 7, 2022
Last update posted
Jul 8, 2024

2021 – 2022

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Integrated Therapeutic Solutions USA, Inc. Newport Beach California 92603
Integrated Therapeutic Solutions USA, Inc. Miami Florida 33126
Integrated Health Solutions USA, Inc. Atlanta Georgia 30363
Integrated Therapeutic Solutions USA, Inc Hazlehurst Georgia 31539
Integrated Therapeutic Solutions USA, Inc. Chicago Illinois 60611
Integrated Therapeutic Solutions USA, Inc Prospect Kentucky 40059
Integrated Therapeutic Solutions USA, Inc Frederick Maryland 21702
Integrated Therapeutic Solutions USA, Inc Gaithersburg Maryland 20878
Integrated Therapeutic Solutions USA, Inc Rockville Maryland 20850
Integrated Therapeutic Solutions USA, Inc Dearborn Michigan 48120
Integrated Therapeutic Solutions USA, Inc. Newark New Jersey 07102
Integrated Therapeutic Solutions USA, Inc. New York New York 10005
Integrated Therapeutic Solutions USA, Inc. Huntingdon Pennsylvania 16652
Integrated Therapeutic Solutions USA, Inc. Charleston South Carolina 29414
Integrated Therapeutic Solutions USA, Inc. Dallas Texas 75219

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05077969, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 8, 2024 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05077969 live on ClinicalTrials.gov.

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