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NCT Number: NCT07725380

Domatinostat With Sirolimus for Relapsed, Refractory Sarcoma and Osteosarcoma

This is a multicenter, open-label, Phase 1/2 study evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and antitumor activity of domatinostat in combination with sirolimus in adolescents and adults with relapsed or refractory sarcoma and osteosarcoma.

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Key information

Age range

12 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Moffitt Cancer Center, Tampa, Florida, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥12 and ≤40 years.
  • Histologically confirmed relapsed or refractory sarcoma (Phase 1) or osteosarcoma (Phase 2).
  • At least one prior standard systemic therapy regimen.
  • Not candidates for available therapies known to provide survival benefit.
  • Karnofsky/Lansky performance score ≥60.
  • Life expectancy ≥16 weeks.
  • Adequate organ function: ANC ≥1,000/mcL, Platelets ≥100,000/uL, Hemoglobin ≥8 g/dL, Adequate hepatic and renal function.
  • Ability to swallow tablets.
  • Negative pregnancy test for females of childbearing potential.
  • Agreement to use effective contraception.
  • Ability to provide informed consent/assent.

Exclusion criteria

  • Receiving another investigational agent.
  • Receiving concurrent anticancer therapy.
  • Known hypersensitivity to domatinostat or sirolimus.
  • Bone marrow-only disease.
  • CNS metastatic disease.
  • Major surgery within 2 weeks prior to treatment.
  • Active malignancy within the previous 3 years (with protocol-specified exceptions).
  • History of solid organ transplantation.
  • Significant recent cardiac disease.
  • Concurrent prohibited CYP3A4/P-gp interacting medications.
  • Uncontrolled infection or other serious uncontrolled illness.
  • Pregnancy or breastfeeding.
  • HIV infection on antiretroviral therapy.
  • Weight <40 kg.
  • Inability to comply with study requirements.

Treatment and study plan

Domatinostat

Drug

Tablet

sirolimus

Drug

Tablet

Primary outcomes

  1. Phase 1: Maximum Tolerated Dose (MTD)

    Time frame: 28 days

    For the phase 1 portion, a standard 3+3 design will be used to determine the MTD and/or RP2D for the Phase 2 portion of this study.

  2. Phase 2: Arm A Event Free Surival

    Time frame: 12 months

    Event free survival (EFS) is defined as the duration of time from start of treatment to time of disease progression, secondary malignancy, or death, whichever occurs first.

  3. Phase 2: Arm B Event Free Surival

    Time frame: 4 months

    Event free survival (EFS) is defined as the duration of time from start of treatment to time of disease progression, secondary malignancy, or death, whichever occurs first.

Secondary outcomes

  1. Phase 2: Overall Survival

    Time frame: Up to 5 years

    Overall Survival (OS) of phase 2 participants.

Study contacts

Contact information is provided by the study sponsor or research team.

Jessica Crimella

CONTACT

[email protected]

813-745-6250

Sponsors and collaborators

Lead sponsor

H. Lee Moffitt Cancer Center and Research Institute

Other

Collaborators

  • Healx USA, Inc
  • National Pediatric Cancer Foundation

Registry information

Official study title

Open-Label, Cohort-Sequential Dose-Escalation and Dose-Confirmation Phase 1/2 Clinical Trial to Evaluate the Safety and Efficacy of Domatinostat in Combination With Sirolimus in Adolescents and Adults With Relapsed, Refractory Sarcoma and Osteosarcoma

Important dates

Study start
2026
Primary completion
2031
Study completion
2031
First posted
Jul 24, 2026
Registry last updated
Jul 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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