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Low-Dose Sirolimus for the Treatment of RUNX1 Familial Platelet Disorder

7. oktober 2026 oppdatert av: Curtis Lachowiez, OHSU Knight Cancer Institute

Low-Dose Sirolimus to Increase Hematopoietic Function in Patients With RUNX1 Familial Platelet Disorder - Part II

This phase I trial studies the safety and side effects of low-dose sirolimus in treating patients with RUNX1 familial platelet disorder (FPD). RUNX1-FPD is a rare inherited disorder with symptoms such as mild to moderately low platelet count, abnormal platelet function, and an increased risk of developing cancers like myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). It is caused by changes (variants) in the RUNX1 gene that is passed down (inherited) from an affected parent. Sirolimus is typically given to help prevent organ rejection in patients receiving kidney transplants. However, sirolimus may also be able to prevent RUNX1-FPD from progressing to cancers like MDS and AML by targeting another protein called mTORC1. Sirolimus may be a safe treatment for patients with RUNX1-FPD.

Studieoversikt

Detaljert beskrivelse

PRIMARY OBJECTIVE:

I. Evaluate the safety and tolerability of low-dose sirolimus in patients with RUNX1 familial platelet disorder (RUNX1-FPD).

SECONDARY OBJECTIVES:

I. Evaluate platelet counts. II. Evaluate changes in somatic mutation variant allele frequency (VAF). III. Evaluate somatic mutation acquisition (i.e., mutation burden). IV. Evaluate the change in platelet function. V. Evaluate the change from baseline in bleeding score (International Society on Thrombosis and Haemostasis Bleeding Assessment Tool [ISTH-BAT]).

VI. Evaluate the change in mTORC1 downstream signaling.

EXPLORATORY OBJECTIVES:

I. Evaluate the rescue of elevated cytokine profiles. II. Evaluate the reversal of myeloid skewing using colony formation assay. III. Evaluate monocytes using clinical flow cytometry. IV. Evaluate changes in patient-reported quality of life (QoL) outcomes measures (e.g., Patient-Reported Outcomes-Common Terminology Criteria for Adverse Events [PRO-CTCAE]).

V. Determine the pharmacokinetics of sirolimus in participants with RUNX1-FPD. VI. Evaluate the correlation between sirolimus trough levels and each endpoint. VII. Make bone marrow smears and bone marrow biopsy slides. VIII. Evaluate the cellularity of bone marrow after study treatment.

OUTLINE:

Patients receive sirolimus orally (PO) once daily (QD) on days 1-168 in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and bone marrow biopsy and/or aspiration throughout the study.

After completion of study treatment, patients are followed for 6 months.

Studietype

Intervensjonell

Registrering (Antatt)

6

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

  • Navn: Knight Cancer Institute Clinical Trials Information
  • Telefonnummer: 503-494-1080
  • E-post: trials@ohsu.edu

Studiesteder

    • Oregon
      • Portland, Oregon, Forente stater, 97239
        • Rekruttering
        • OHSU Knight Cancer Institute
        • Hovedetterforsker:
          • Curtis A. Lachowiez
        • Ta kontakt med:
          • Knight Cancer Institute Clinical Trials Information
          • Telefonnummer: 503-494-1080
          • E-post: trials@ohsu.edu

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Patient has provided signed, informed consent before initiation of any study specific procedures
  • Aged ≥ 18 years at the time of signing the informed consent
  • Confirmed pathogenic/likely pathogenic (P/LP) germline RUNX1 variant per ClinGen Myeloid Malignancy Variant Curation Expert Panel (MM-VCEP) RUNX1-specific variant curation rules
  • Patient must be willing to provide a bone marrow sample at time of screening and at the end of treatment with sirolimus
  • Platelet count of ≥ 50,000/µL
  • Creatinine clearance (CrCl) of ≥ 60 mL/min; estimated using the Cockcroft Gault formula or measured by 24 hour urine collection. Exceptions will be allowed, at the discretion of the investigator, for cases of a concomitant medication that alters renal function
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 3 × upper limit of normal (ULN)
  • Total bilirubin < 1.5 × ULN
  • Left ventricular ejection fraction (EF) > 50% or at the discretion of the investigator

Exclusion Criteria:

  • Known allergy to sirolimus

  • History of major bleeding events that are clinically relevant in the judgement of the investigator or non-major bleeding events that cannot be controlled using SOC practices

  • Any known history of lymphoma, myelodysplastic syndrome (MDS), or other hematologic malignancy using International Working Group criteria

  • Prior treatment with sirolimus or a rapalog, mTOR inhibitor, or B-cell-depleting therapy within 28 days before study day 1

  • Treatment with strong inhibitors of cytochrome P450 3A4 (CYP3A4; e.g., ketoconazole, voriconazole, itraconazole, erythromycin, telithromycin, and clarithromycin), strong inducers of CYP3A4 (e.g., rifampin and rifabutin), other drugs that could increase sirolimus blood concentrations (e.g., bromocriptine, cimetidine, cisapride, clotrimazole, danazol, diltiazem, fluconazole, letermovir, protease inhibitors [e.g., ritonavir, indinavir, boceprevir, and telaprevir], metoclopramide, nicardipine, troleandomycin, and verapamil), other drugs that could decrease sirolimus blood concentrations (e.g., carbamazepine, phenobarbital, phenytoin, rifapentine, St. John's Wort [Hypericum perforatum]), or drugs with blood concentrations that could increase (e.g., verapamil) within 7 days before study day 1, or at the discretion of the investigator

  • Use of cannabidiols that increase blood levels of sirolimus, within 7 days before study day 1 or at the discretion of the investigator

  • Myocardial infarction within 6 months before study day 1, congestive heart failure (New York Heart Association > class II)

  • Total cholesterol > 300 mg/dL or triglyceride > 400 mg/dL

  • Arterial thrombosis (e.g., stroke or transient ischemic attack) within 6 months before study day 1

  • Infection requiring intravenous anti-infective treatment within 1 week of study day 1

  • Live vaccines (e.g., measles, mumps, rubella, oral polio, Bacillus Calmette-Guerin [BCG], yellow fever, varicella, and TY21a typhoid) within 28 days before study day 1

  • Known diagnosis of tuberculosis is exclusionary to provide protection against reactivation of infections by the immunosuppressive activity of the study drug sirolimus

    • The enrollment of a patient with a history of infection with hepatitis B virus (HBV) but with undetectable HBV deoxyribonucleic acid (DNA) by standard institutional testing can be considered after consultation with the investigator
    • Patients with history of chronic hepatitis C virus (HCV) must have documentation of completed curative standard of care (SOC) antiviral therapy
    • Patients with history of HIV infection must be well-managed with SOC antiretroviral therapy (highly active antiretroviral therapy [HAART])
    • Patients with history of Epstein-Barr may be considered after consultation with the treating physician
  • Participants who are pregnant may become pregnant, or who are breastfeeding

    • Because adequate and well-controlled studies of the impact of sirolimus on fetuses currently do not exist, study approved contraception must be used from start of study therapy to 12 weeks after the last dose of sirolimus
    • Adequate and well-controlled studies of infants fed breastmilk from patients undergoing sirolimus therapy do not exist and breastfeeding during study treatment is prohibited

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Treatment (sirolimus)

Patients receive sirolimus PO QD on days 1-168 in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and bone marrow biopsy and/or aspiration throughout the study.

Ancillary studies

Undergo collection of blood

Andre navn:
  • Biologisk prøvesamling
  • Bioprøve samlet
  • Prøvesamling

Undergo bone marrow biopsy/aspiration

Undergo bone marrow biopsy/aspiration

Andre navn:
  • Biopsi av benmarg
  • Biopsi, benmarg

Given PO

Andre navn:
  • Rapamycin
  • Rapamune
  • AY 22989
  • RAPA
  • SILA 9268A
  • WY-090217
  • AY-22989
  • AY22989
  • SILA-9268A
  • SILA9268A
  • WY 090217
  • WY090217

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence of grade 3+ treatment-related adverse events (TRAEs)
Tidsramme: From study day 1 (week 1) to 30 days after the last dose of sirolimus

The incidence of grade 3+ TRAEs and the total proportion of participants who experienced grade 3+ TRAEs will be estimated and presented with the corresponding 95% exact Clopper Pearson confidence intervals.

From study day 1 (week 1) to 30 days after the last dose of sirolimus

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in platelet count
Tidsramme: From screening, pre dose on study day 1 (week 1) to end of treatment (EOT) (week 24, day 168)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to end of treatment (EOT) (week 24, day 168)
Change in variant allele frequency for existing clones
Tidsramme: From screening to end of study (EOS) (week 52, day 365)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening to end of study (EOS) (week 52, day 365)
Change in number of clonal hematopoiesis of indeterminate potential mutations
Tidsramme: From screening to EOS (week 52, day 365)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening to EOS (week 52, day 365)
Change in percent positivity based on activated GPIIb IIIa and surface P selectin and CD42b
Tidsramme: From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
Change in aggregation from baseline based on thromboelastography (TEG)
Tidsramme: From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
Change in the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool score
Tidsramme: From study day 1 (week 1) to EOS (week 52, day 365)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From study day 1 (week 1) to EOS (week 52, day 365)
Change in the relative amount of the protein 4eBP1
Tidsramme: From screening, pre dose on study day 1 (week 1) to EOS (week 52, day 365)

Will be based on flow cytometry and immunohistochemistry assays. Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to EOS (week 52, day 365)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Curtis A Lachowiez, OHSU Knight Cancer Institute

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

5. oktober 2026

Primær fullføring (Antatt)

30. juni 2030

Studiet fullført (Antatt)

31. desember 2030

Datoer for studieregistrering

Først innsendt

21. september 2026

Først innsendt som oppfylte QC-kriteriene

21. september 2026

Først lagt ut (Faktiske)

28. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

7. oktober 2026

Sist bekreftet

1. oktober 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • STUDY00028610
  • P30CA069533 (U.S. NIH-stipend/kontrakt)
  • NCI-2026-03902 (Registeridentifikator: CTRP (Clinical Trial Reporting Program))
  • STUDY00028610 (Annen identifikator: OHSU Knight Cancer Institute)

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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