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Completed Phase 3 Interventional Accepts healthy volunteers

CCT-102 or Expectant Management in Delayed Pregnancy Loss

ClinicalTrials.gov ID: NCT06121063

Public ClinicalTrials.gov record NCT06121063. 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 Jul 21, 2026, 12:15 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

The Efficacy and Safety of a CCT-102 Regimen or Expectant Management in the Treatment of First Trimester Pregnancy Loss

Study identification

NCT ID
NCT06121063
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Conceptra Biosciences, LLC
Industry
Enrollment
183 participants

Conditions and interventions

Interventions

  • CCT-102 A and CCT-102 B Combination Product

Combination Product

Eligibility (public fields only)

Age range
18 Years to 50 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Jul 20, 2023
Primary completion
May 14, 2025
Completion
Jul 29, 2025
Last update posted
Aug 21, 2025

2023 – 2025

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Noble Clinical Research Tucson Arizona 85704
Amicis Research Center, LLC San Fernando California 91340
Emerald Coast Obstetrics and Gynecology Panama City Florida 32405
Cypress Medical Research Center Wichita Kansas 67226
Sinai Hospital of Baltimore Baltimore Maryland 21215
Las Vegas Clinical Trials Las Vegas Nevada 89030
Columbia University Irving Medical Center New York New York 10032
Montefiore Medical Center The Bronx New York 10461
Eastern Carolina Women's Center, PA New Bern North Carolina 28562
Lyndhurst Clin Research Winston-Salem North Carolina 27103
Penn State Hershey Obstetrics and Gynecology Hershey Pennsylvania 17033
The University of Texas Medical Branch at Galveston Galveston Texas 77555
Maximos Obstetrics & Gynecology League City Texas 77573
Prime Clinical Research - Lewisville North Valley Lewisville Texas 75067
Tidewater Clinical Research Virginia Beach Virginia 23456

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 NCT06121063, 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 Aug 21, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06121063 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →