Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06930664 · ClinicalTrials.gov registry record · Phase 1

A Study of Sotatercept (MK-7962) in Healthy Females Administered as a Liquid Formulation in an Autoinjector Versus the Lyophilized Formulation (MK-7962-027)

A Phase 1 study, sponsored by Merck Sharp & Dohme.

Completed
Registry status
Phase 1
Development phase
146
Enrollment target

NCT06930664: Completed Phase 1 study, sponsored by Merck Sharp & Dohme.

NCT06930664 is a Phase 1 study that has completed, run by Merck Sharp & Dohme. The registered enrollment target is 146 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (143% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06930664, a Phase 1 study, has completed, sponsored by Merck Sharp & Dohme.

COMPLETED
Registry status
Phase 1
Development phase
146 participants
Enrollment target

Study Summary

The goal of the study is to learn what happens to different forms of sotatercept medications in a healthy person's body over time. Researchers want to know if there is a difference in the healthy person's body when different forms of sotatercept medications are given.

Primary Outcome

Blood samples will be collected to determine the AUC0-inf of sotatercept in plasma.

Interventions

  • BIOLOGICAL Sotatercept
  • BIOLOGICAL Sotatercept Autoinjector

Trial Details

FieldValue
Enrollment Target 146 participants
Start Date 2025-05-16
Est. Completion 2025-11-25
Phase Phase 1
Merck Sharp & Dohme

558 total trials

What the finished NCT06930664 record still lists

NCT06930664 is an interventional study that assigns participants to a tested intervention. The registered 146 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (143% higher).

The record links to 0 conditions, and to 2 interventions - of which Sotatercept is the first listed.

NCT06930664 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06930664 about?

NCT06930664 is a clinical study titled "A Study of Sotatercept (MK-7962) in Healthy Females Administered as a Liquid Formulation in an Autoinjector Versus the Lyophilized Formulation (MK-7962-027)". The goal of the study is to learn what happens to different forms of sotatercept medications in a healthy person's body over time. Researchers want to know if there is a difference in the healthy person's body when different forms of sotatercept medications are given.

What is the current status of trial NCT06930664?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 146 participants. The study started on 2025-05-16. Estimated completion is 2025-11-25.

What interventions are being tested in trial NCT06930664?

The interventions under investigation include: Sotatercept (BIOLOGICAL), Sotatercept Autoinjector (BIOLOGICAL).

Who is sponsoring clinical trial NCT06930664?

This trial is sponsored by Merck Sharp & Dohme, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06930664's enrollment target sits among peer trials

146 391st of 2000 higher than 1,610 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03490929 · 146 participants · Phase 4

    CEUS for Blunt Abdominal Trauma in Children

  • NCT04755062 · 146 participants · NA

    A Culturally-relevant Micronutrient-dense Plant-rich (mNDPR) Dietary Intervention for Native Americans

  • NCT04867954 · 146 participants

    Development of 4D Flow MRI for Risk Stratification of Variceal Bleeding in Cirrhosis

  • NCT05051618 · 146 participants · NA

    Exercise Training for Managing Major Depressive Disorder in Multiple Sclerosis

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06930664, the US trial registry maintained by the National Library of Medicine. NCT06930664 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.