CONRAD
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
Safety, PK, and PD Study of a Vaginal Insert Containing TAF and EVG
NCT03762772
Safety, PK, and PD Study of IVRs Releasing TFV and LNG
NCT03279120
PK and PD Study of Oral F/TAF for HIV Prevention
NCT02904369
Exploratory Pharmacodynamic Study of Tenofovir-Based Products
NCT02722343
Development of Adherence Biomarkers for Multiple Microbicide and Multipurpose Prevention Technology (MPT) Dosage Forms
NCT02569697
Assessing the Disintegration, Safety, and Acceptability of Placebo Vaginal Inserts for the Delivery of Vaginal Products
NCT02534779
A Safety Study Of The Caya® Diaphragm Used With ContraGel®
NCT02462954
Postcoital Testing Study of the SILCS Diaphragm Used With 3% N-9 Gel, ContraGel, or No Gel
NCT02309554
Comparison of Tenofovir Vaginal Gel and Film Formulations
NCT02280109
Phase I One-month Safety, PK, PD, and Acceptability Study of IVR Releasing TFV and LNG or TFV Alone
NCT02235662
The Role of Vitamin D in Female Reproductive Tract Immunity
NCT02186535
Tenofovir Levels Following Local Application of Tenofovir Reduced-Glycerin 1% Gel
NCT01768962
In Vivo Drug Interaction Pharmacokinetic Study of Tenofovir 1% Gel and Three Commonly Used Vaginal Products
NCT01813162
A Phase I Trial to Assess the Safety of Tenofovir Gel and Film Formulations: FAME 04
NCT01989663
Safety and Acceptability Study of Oral Emtricitabine/Tenofovir Disoproxil Fumarate Tablet and Rectally-Applied Tenofovir Reduced-Glycerin 1% Gel
NCT01687218
Influence of Reproductive Cycle and Menopause on HIV-1 Infection and TFV Gel Activity
NCT01810315
Biomarkers of Protocol Compliance and Product Adherence
NCT01804023
Safety, Pharmacokinetics, Pharmacodynamics, and Disintegration Time of Vaginal Tablets Containing Tenofovir and/or Emtricitabine
NCT01694407
Coital Pharmacokinetics/Pharmacodynamics (PK/PD) of Tenofovir Gel
NCT01687205
Identification of Novel Biomarkers of Cervicovaginal Mucosal Inflammation
NCT01593124
Contraception and Menstrual Cycle Effect on Pharmacokinetics, Pharmacodynamics and Safety in Tenofovir Vaginal Gel Use
NCT01421368
Pharmacokinetic and Pharmacodynamic Study of Tenofovir 1% Gel
NCT01369303
Study of How Bacterial Vaginosis and Its Treatment Affects Cervical and Vaginal Tissue
NCT01347632
Rectal Safety and Acceptability Study of Tenofovir 1% Gel
NCT01232803
Microbicide Safety and Acceptability in Young Men
NCT01283360
Prostate Specific Antigen (PSA) and Acute Failure Modes Study of the PATH Woman's Condom and FC2 Female Condom
NCT01178840
Rectal Microbicide Safety and Acceptability Trial of Topically Applied Tenofovir Compared With Oral Tablet
NCT00984971
Residence Time of Biomarkers of Semen Exposure
NCT00984555
Contraceptive Effectiveness and Safety of the SILCS Diaphragm
NCT00578877
Pharmacokinetic Study of the Vaginal Microbicide Agent 1% Tenofovir Gel
NCT00561496
Study of UC-781 Vaginal Microbicide
NCT00132444
Contraceptive Effectiveness Trial of Cellulose Sulfate Gel
NCT00255294
Postcoital Testing of the SILCS Diaphragm
NCT00561613
Phase Distribution
| Phase | Trial 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.
Read our methodology - how this data is sourced, computed, and verified.
Related
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.