CONRAD

33 total trials 33 completed

CONRAD sponsors 33 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 33 completed. 0 of these trials are in Phase 3-4 (later-stage) and 28 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is HIV Prevention, with 2 trials.

Trial Pipeline

33 total, page 1 of 1

COMPLETED Phase 1

Safety, PK, and PD Study of a Vaginal Insert Containing TAF and EVG

NCT03762772

COMPLETED Phase 1

Safety, PK, and PD Study of IVRs Releasing TFV and LNG

NCT03279120

COMPLETED Phase 1

PK and PD Study of Oral F/TAF for HIV Prevention

NCT02904369

COMPLETED Phase 1

Exploratory Pharmacodynamic Study of Tenofovir-Based Products

NCT02722343

COMPLETED Phase 1

Development of Adherence Biomarkers for Multiple Microbicide and Multipurpose Prevention Technology (MPT) Dosage Forms

NCT02569697

COMPLETED NA

Assessing the Disintegration, Safety, and Acceptability of Placebo Vaginal Inserts for the Delivery of Vaginal Products

NCT02534779

COMPLETED Phase 1

A Safety Study Of The Caya® Diaphragm Used With ContraGel®

NCT02462954

COMPLETED Phase 1

Postcoital Testing Study of the SILCS Diaphragm Used With 3% N-9 Gel, ContraGel, or No Gel

NCT02309554

COMPLETED Early Phase 1

Comparison of Tenofovir Vaginal Gel and Film Formulations

NCT02280109

COMPLETED Phase 1

Phase I One-month Safety, PK, PD, and Acceptability Study of IVR Releasing TFV and LNG or TFV Alone

NCT02235662

COMPLETED Phase 1

The Role of Vitamin D in Female Reproductive Tract Immunity

NCT02186535

COMPLETED Phase 1

Tenofovir Levels Following Local Application of Tenofovir Reduced-Glycerin 1% Gel

NCT01768962

COMPLETED Phase 1

In Vivo Drug Interaction Pharmacokinetic Study of Tenofovir 1% Gel and Three Commonly Used Vaginal Products

NCT01813162

COMPLETED Phase 1

A Phase I Trial to Assess the Safety of Tenofovir Gel and Film Formulations: FAME 04

NCT01989663

COMPLETED Phase 2

Safety and Acceptability Study of Oral Emtricitabine/Tenofovir Disoproxil Fumarate Tablet and Rectally-Applied Tenofovir Reduced-Glycerin 1% Gel

NCT01687218

COMPLETED Phase 1

Influence of Reproductive Cycle and Menopause on HIV-1 Infection and TFV Gel Activity

NCT01810315

COMPLETED

Biomarkers of Protocol Compliance and Product Adherence

NCT01804023

COMPLETED Phase 1

Safety, Pharmacokinetics, Pharmacodynamics, and Disintegration Time of Vaginal Tablets Containing Tenofovir and/or Emtricitabine

NCT01694407

COMPLETED Phase 1

Coital Pharmacokinetics/Pharmacodynamics (PK/PD) of Tenofovir Gel

NCT01687205

COMPLETED Phase 2

Identification of Novel Biomarkers of Cervicovaginal Mucosal Inflammation

NCT01593124

COMPLETED Phase 1

Contraception and Menstrual Cycle Effect on Pharmacokinetics, Pharmacodynamics and Safety in Tenofovir Vaginal Gel Use

NCT01421368

COMPLETED Phase 1

Pharmacokinetic and Pharmacodynamic Study of Tenofovir 1% Gel

NCT01369303

COMPLETED NA

Study of How Bacterial Vaginosis and Its Treatment Affects Cervical and Vaginal Tissue

NCT01347632

COMPLETED Phase 1

Rectal Safety and Acceptability Study of Tenofovir 1% Gel

NCT01232803

COMPLETED Phase 1

Microbicide Safety and Acceptability in Young Men

NCT01283360

COMPLETED NA

Prostate Specific Antigen (PSA) and Acute Failure Modes Study of the PATH Woman's Condom and FC2 Female Condom

NCT01178840

COMPLETED Phase 1

Rectal Microbicide Safety and Acceptability Trial of Topically Applied Tenofovir Compared With Oral Tablet

NCT00984971

COMPLETED

Residence Time of Biomarkers of Semen Exposure

NCT00984555

COMPLETED Phase 2

Contraceptive Effectiveness and Safety of the SILCS Diaphragm

NCT00578877

COMPLETED Phase 1

Pharmacokinetic Study of the Vaginal Microbicide Agent 1% Tenofovir Gel

NCT00561496

COMPLETED Phase 1

Study of UC-781 Vaginal Microbicide

NCT00132444

COMPLETED Phase 2

Contraceptive Effectiveness Trial of Cellulose Sulfate Gel

NCT00255294

COMPLETED Phase 1

Postcoital Testing of the SILCS Diaphragm

NCT00561613

Phase Distribution

PhaseTrial count
Phase 1 24
Phase 2 4

Therapeutic Areas

What the Pipeline for CONRAD Shows

According to the ClinicalTrials.gov registry, CONRAD is linked to 33 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 33 are already marked complete, representing roughly 100% of the total.

The phase mix for CONRAD reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 28 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for CONRAD is HIV Prevention with 2 linked trials, and 3 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.