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NCT05739123 · ClinicalTrials.gov registry record

Relugolix Pregnancy Registry: An Observational Study of the Safety of Relugolix-Containing Therapy Exposure in Pregnant Women and Their Offspring

A clinical trial of Pregnancy Related and Pregnancy Complications, sponsored by Sumitomo Pharma Switzerland.

Recruiting
Registry status
728
Enrollment target
1
Study location

NCT05739123 is a study of Pregnancy Related and Pregnancy Complications that is actively recruiting participants, run by Sumitomo Pharma Switzerland. The registered enrollment target is 728 participants, below the 1,956-participant average among 99 other Pregnancy Related trials with a reported enrollment target (63% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05739123, a study of Pregnancy Related and Pregnancy Complications, is actively recruiting participants, sponsored by Sumitomo Pharma Switzerland.

RECRUITING
Registry status
728 participants
Enrollment target
1
Study location

Study Summary

The Relugolix Pregnancy Registry is a prospective, observational cohort study designed to evaluate the association between relugolix-containing therapy exposure during pregnancy and subsequent maternal, fetal, and infant outcomes. Data will be collected from enrolled pregnant women and the healthcare providers (HCPs) involved in their care or the care of their infants, if applicable.

Interventions

  • DRUG Relugolix-Containing Product

Study Locations (1)

North Carolina

  • PPD - Wilmington

Trial Details

FieldValue
Enrollment Target 728 participants
Start Date 2023-05-08
Est. Completion 2033-05

Sponsor

Sumitomo Pharma Switzerland

13 total trials

What the Registry Record Tells You About NCT05739123

The ClinicalTrials.gov registry entry for NCT05739123 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 728 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,956-participant average among 99 other Pregnancy Related trials with a reported enrollment target (63% lower). The listed sponsor is Sumitomo Pharma Switzerland, which has 13 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Pregnancy Related appearing as the primary indexed condition, and to 1 intervention - of which Relugolix-Containing Product is the first listed.

NCT05739123 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT05739123 about?

NCT05739123 is a clinical study titled "Relugolix Pregnancy Registry: An Observational Study of the Safety of Relugolix-Containing Therapy Exposure in Pregnant Women and Their Offspring". The Relugolix Pregnancy Registry is a prospective, observational cohort study designed to evaluate the association between relugolix-containing therapy exposure during pregnancy and subsequent maternal, fetal, and infant outcomes. Data will be collected from enrolled pregnant women and the healthcar...

What is the current status of trial NCT05739123?

This trial is currently recruiting. The enrollment target is 728 participants. The study started on 2023-05-08. Estimated completion is 2033-05.

What conditions does trial NCT05739123 study?

This clinical trial studies the following conditions: Pregnancy Related, Pregnancy Complications, Pregnancy, High Risk.

What interventions are being tested in trial NCT05739123?

The interventions under investigation include: Relugolix-Containing Product (DRUG).

Who is sponsoring clinical trial NCT05739123?

This trial is sponsored by Sumitomo Pharma Switzerland, which has 13 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05739123 being conducted?

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

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

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