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RECRUITING Phase 1

Study to Assess Safety and Efficacy of Vactosertib in Adolescents and Adults With Recurrent, Refractory or Progressive Osteosarcoma

NCT05588648 · View on ClinicalTrials.gov ↗

Study Summary

MP-VAC-209 is a Phase I/II, open label, single arm, multi-center study to assess safety, tolerability, and antitumor activity of vactosertib as a single agent in adolescents and adults with recurrent, refractory, or progressive osteosarcoma. Vactosertib is given orally, twice a day, to people 12 years of age and older who meet the criteria for study enrollment.

Conditions Studied

Interventions

  • DRUG Vactosertib

Study Locations (3)

Other

  • National Cancer Center — Gyeonggi-do
  • Korea Institute of Radiological & Medical Sciences — Seoul

Ohio

  • UH Rainbow Babies & Children's Hospital — Cleveland

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2023-05-01
Est. Completion 2025-12
Phase Phase 1

Sponsor

MedPacto

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05588648

The ClinicalTrials.gov registry entry for NCT05588648 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MedPacto, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Osteosarcoma appearing as the primary indexed condition, and to 1 intervention — of which Vactosertib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05588648 reports 3 study locations spanning 2 distinct geographic areas — top geographies include Other, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05588648 about?

NCT05588648 is a clinical study titled "Study to Assess Safety and Efficacy of Vactosertib in Adolescents and Adults With Recurrent, Refractory or Progressive Osteosarcoma". MP-VAC-209 is a Phase I/II, open label, single arm, multi-center study to assess safety, tolerability, and antitumor activity of vactosertib as a single agent in adolescents and adults with recurrent, refractory, or progressive osteosarcoma. Vactosertib is given orally, twice a day, to people 12 yea...

What is the current status of trial NCT05588648?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2023-05-01. Estimated completion is 2025-12.

What conditions does trial NCT05588648 study?

This clinical trial studies the following conditions: Osteosarcoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05588648?

The interventions under investigation include: Vactosertib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05588648?

This trial is sponsored by MedPacto, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05588648 being conducted?

This trial has 3 study locations across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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