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MyelofibrosisPhase 1/2MPN-RC 129NCT07734077

Revumenib in Patients With Myelofibrosis

A Phase 1/2 study testing Revumenib, Ruxolitinib and FEDRATINIB in people with Myelofibrosis and Post-polycythemia Vera Myelofibrosis, run by John Mascarenhas at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This is a Phase Ib/II 2 study investigating the safety and efficacy of revumenib in two cohorts of participants with myelofibrosis. COHORT-1 will investigate the safety of revumenib as monotherapy in participants with myelofibrosis previously treated with a JAK inhibitor. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Revumenib, Ruxolitinib and FEDRATINIB
Could I receive a placebo?
No, everyone receives an active treatment
How many people
32 participants
Where
1 siteUnited States
Study dates
1 Dec 2026to 1 Dec 2028
Phase
Phase 1/2
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • In order to be eligible to participate in this study, an individual must meet all of the following criteria:
  • Adults ≥ 18 years of age at time of signing the informed consent
  • Participants must voluntarily sign informed consent form (ICF) and be willing and able to adhere to the study visit schedule and all protocol requirements.
  • Have an Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
  • Participants must have a pathologically confirmed diagnosis of PMF, post-ET-MF or post-PV-MF as per the WHO diagnostic criteria, with intermediate-1 or higher risk disease by DIPSS (14.1).
  • Criteria for COHORT-1 (Monotherapy): Treated with at least one prior line of JAK inhibitor therapy to which they were refractory/resistant, lost response, or intolerant, or is not a candidate for approved JAK inhibitor therapy per investigator judgement, and with one or more of the following features of active disease:
Show all 56Show fewer
  • Spleen palpable ≥ 5 cm below the left costal margin or > 450cm3 by MRI/CT
  • MPN-SAF TSS ≥ 10
  • Transfusion dependence (requiring at least 6 units of PRBCs in the 12 weeks prior to study enrollment, for a hemoglobin < 8.5g/dL in the absence of bleeding or treatment-induced anemia)
  • Criteria for COHORT-2 (Combination therapy): Currently receiving treatment with an approved JAK inhibitor (including ruxolitinib, fedratinib, or momelotinib) with stable dose for at least 12 weeks prior to study enrollment, and with one or more of the following features of active disease:
  • Spleen palpable ≥ 5 cm below the left costal margin or > 450cm3 by MRI/CT
  • MPN-SAF TSS ≥ 10
  • Transfusion dependence (requiring at least 6 units of PRBCs in the 12 weeks prior to study enrollment, for a hemoglobin < 8.5g/dL in the absence of bleeding or treatment-induced anemia)
  • Adequate organ function as demonstrated by the following within 28 days prior to Cycle 1 Day 1:
  • ALT (SGPT) and/or AST (SGOT) < 3 × the upper limit of normal (ULN), or < 5 × ULN if, upon judgment of the treating physician, it is believed to be due to MF-related extramedullary hematopoiesis (EMH);
  • Total bilirubin < 3 × ULN for age (< 4 x ULN for age if attributed to MF related EMH or Gilbert's syndrome)
  • Creatinine clearance ≥ 30 mL/min by Cockcroft Gault formula;
  • Prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤ 1.5 × upper limit of normal (ULN)
  • Adequate cardiac function defined as ejection fraction of ≥50% by echocardiogram or multigated acquisition (MUGA) scan
  • Bone marrow and/or peripheral blood blast count < 10%;
  • Absolute neutrophil count (ANC) ≥ 1000 mm3; and
  • Platelet count ≥ 75 x 109/L at time of enrollment
  • QTcF ≤ 450msec at screening
  • Recovery to ≤ Grade 1 or baseline of any toxicities due to prior systemic treatments, excluding alopecia
  • Life expectancy of at least six months
  • Females of childbearing potential must have a negative serum pregnancy test at Screening and a negative urine or serum pregnancy test within 72 hours before the initiation of protocol therapy. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be obtained. Participants are considered to be not of childbearing potential if they are considered to be post-menopausal or surgically sterilized (eg, , hysterectomy, bilateral salpingectomy). Females who have been amenorrheic for at least 12 or more months are still considered to be of childbearing potential if the amenorrhea is possibly due to prior chemotherapy, anti-estrogens, ovarian suppression or any other reversible reason.
  • Females of childbearing potential must be willing to use a highly effective method of contraception from the time of first study intervention dose through the required contraceptive period (4 months following the last dose of study drug) and must be willing to refrain from in vitro fertilization and egg donation during the required contraceptive period.
  • Males must be surgically sterile or agree to use barrier contraception (male condoms) from the time of first study intervention dose through the required contraceptive period of 4 months after last dose of study drug. Males must be willing to refrain from sperm donation during the required contraceptive period.
  • Able to adhere to the study visit schedule and all protocol requirements Exclusion Criteria
  • An individual who meets any of the following criteria will be excluded from participation in this study:
  • Treatment with any MF-directed therapy (including investigational therapies) within 2 weeks or 5 half-lives, whichever is shorter, of Cycle 1 Day 1
  • Participants in COHORT-1 should not have received a JAK inhibitor within 14 days prior to Cycle 1 Day 1. Participants who remain on JAK inhibitor at time of screening should be tapered off per investigator discretion.
  • Hydroxyurea is permitted until the day prior to C1D1, if needed for disease control.
  • Undergone allogeneic hematopoietic stem cell transplant (allo-HSCT) within the last 6 months prior to enrollment, or with active GVHD and/or on immunosuppressive therapy.
  • Not currently a candidate for allo-HSCT, per investigator discretion. Patients who are not willing to undergo transplantation or for whom a suitable donor is not available are considered as transplant ineligible.
  • Prior splenectomy, splenic irradiation, or splenic artery embolization within 6 months of C1D1
  • GI disease meeting any of the following criteria:
  • Impairment of GI function that could significantly alter the absorption of revumenib (eg. Gastric bypass, gastroparesis)
  • Cirrhosis with a Child-Pugh score of B or C, or National Cancer Institute (NCI) Organ Dysfunction Working Group category of Severe Dysfunction
  • Inability to swallow oral medications
  • Any of the following cardiac abnormalities:
  • Any of the following within the 6 months before study entry: myocardial infarction, uncontrolled/unstable angina, congestive heart failure (New York Heart Association Class ≥II), life-threatening, uncontrolled arrhythmia, cerebrovascular accident or transient ischemic attack. Participants with controlled atrial fibrillation are allowed to enroll
  • QTcF (Fridericia's correction) > 450ms at screening
  • Diagnosis of suspicion of Long QT syndrome or family history of Long QT syndrome
  • Recipient of organ transplant
  • Other malignancy within the last three years, other than curatively treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, organ-confined or treated non-metastatic prostate cancer with normal prostate-specific antigen, in situ breast carcinoma after complete surgical resection, or superficial/non-invasive transitional cell bladder carcinoma.
  • Presence of uncontrolled active infection of any type. Mild to moderate localized infections under control with antibiotic treatment are acceptable for study entry. Patients with ongoing serious infection are not eligible regardless of antimicrobial therapy. Prophylactic antibiotics are acceptable per NCCN infection guidelines.
  • If participant is known to be human immunodeficiency virus (HIV)-positive, they must have an undetectable HIV viral load within the previous 6 months. If viral load testing has not been performed within the previous 6 months, it much be performed during screening.
  • Known active or chronic hepatitis B, or active hepatitis C infection. Participants with a history of HCV infection who have completed curative therapy for HCV at least 12 weeks before the Screening Visit and have a documented undetectable viral load at the Screening Visit are eligible for inclusion.
  • The following exclusions apply related to concomitant use of CYP3A4 inhibitors and inducers:
  • Participants who will not receive revumenib with coadministration of a strong CYP3A4i (eg, itraconazole, ketoconazole, posaconazole, or voriconazole) must discontinue all strong CYP3A4 inhibitors at least 7 days or 5 half-lives, whichever is longer, before the first dose of revumenib. They will receive goal dose of revumenib 270 mg Q12h and they may continue to receive moderate or weak CYP3A4 inhibitors, including fluconazole and isavuconazole.
  • Participants who will receive revumenib with coadministration of a strong CYP3A4i (eg, itraconazole, ketoconazole, posaconazole, or voriconazole) must have started the treatment at least 24 hours before the first dose of revumenib. They will receive goal dose of revumenib 160 mg Q12h.
  • Concomitant use of a strong or moderate CYP3A4 inducer is prohibited while on study. Strong or moderate inducers of CYP3A4 should be discontinued at least five half-lives or 14 days (whichever is longer) prior to the first dose of revumenib.
  • Participants requiring the concurrent use of medications known or suspected to prolong the QT/QTc interval, with the exception of drugs with low risk of QT/QTc prolongation that are used as standard supportive therapies (eg, diphenhydramine, famotidine, ondansetron, sulfamethoxazole and trimethoprim) and the azoles permitted. Females who are pregnant or lactating.
  • Any serious, unstable medical or psychiatric condition that would prevent (as judged by the Investigator) the participant from signing the informed consent form or any condition, including the presence of laboratory abnormalities and inability to swallow pills, which places the participant at unacceptable risk if they were to participate in the study or confounds the ability to interpret data from the study.
  • Is or has an immediate family member (e.g., spouse, parent/legal guardian, sibling, or child) who is investigational site or sponsor staff directly involved with this trial, unless prospective IRB approval (by chair or designee) is given allowing exception to this criterion for a specific participant.

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Gillian Sanchez contact

(212) 241-1391

gillian.sanchez@mssm.edu

Shakira Forde contact

shakira.forde@mssm.edu

United States1 site

  • Icahn School of Medicine at the Mount Sinai Hospital

    New York, New York, 10029

    Gillian Sanchez, gillian.sanchez@mssm.edu

    Gabriela Bello, gabriela.bello@mssm.edu

Other trials in United States

About this study

Official title: Phase Ib/II Study Of Revumenib As Monotherapy Or In Combination With Jak Inhibitors In Patients With Myelofibrosis

This is a Phase Ib/II 2 study investigating the safety and efficacy of revumenib in two cohorts of participants with myelofibrosis. COHORT-1 will investigate the safety of revumenib as monotherapy in participants with myelofibrosis previously treated with a JAK inhibitor. Following confirmation of safety in COHORT-1, the study will proceed with enrollment in COHORT-2, which will evaluate the efficacy and safety of revumenib in combination with a JAK inhibitor.

Read the detailed description

This is a Phase Ib/II 2 study investigating the safety and efficacy of revumenib in two cohorts of participants with myelofibrosis. COHORT-1 will investigate the safety of revumenib as monotherapy in participants with myelofibrosis previously treated with a JAK inhibitor. Following confirmation of safety in COHORT-1, the study will proceed with enrollment in COHORT-2, which will evaluate the efficacy and safety of revumenib in combination with a JAK inhibitor. COHORT-2 will enroll participants on stable dose of a JAK inhibitor (ruxolitinib, fedratinib, or momelotinib) for at least 12 weeks at time of enrollment and who demonstrate suboptimal response as evidenced by persistent splenomegaly, symptoms or transfusion-dependent anemia, with revumenib added to existing JAK inhibitor therapy. The researchers hypothesize that revumenib will demonstrate a favorable safety profile in myelofibrosis participants, and demonstrate clinical activity (response of CR, PR or CI by IWG-MRT and ELN criteria) in participants with suboptimal response to a JAK inhibitor.

Being tested
Revumenib, Ruxolitinib, FEDRATINIB, Momelotinib
Keywords
Myelofibrosis, Revumenib, JAK inhibitor
Medical subject headings
Primary Myelofibrosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • RevumenibDrug

    Also called Revuforj)

    Dose Level 1: Revumenib 160mg twice daily or 110mg twice daily

    Dose Level 2: Revumenib 270mg twice daily or 160mg twice daily

  • RuxolitinibDrug

    Part of routine care. Participants to continue on dosage as prescribed by provider, 5 to 20 mg BID

  • FEDRATINIBDrug

    Part of routine care. Participants to continue on dosage as prescribed by provider, 100 mg to 400 mg daily.

  • MomelotinibDrug

    Part of routine care. Participants to continue on dosage as prescribed by provider, 100 mg to 200 mg daily.

Study groups in NCT07734077
Study groupRoleWhat they receive
COHORT-1 (revumenib monotherapy)ExperimentalRevumenib monotherapy utilizing a 3+3 dose-escalation design
Receives: Drug: Revumenib
COHORT-2 (revumenib added to JAK inhibitor therapy)ExperimentalDosage of revumenib from Cohort 1 plus JAK inhibitor therapy (ruxolitinib, fedratinib, or momelotinib)
Receives: Drug: Revumenib; Drug: Ruxolitinib; Drug: FEDRATINIB; Drug: Momelotinib

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Dose limiting toxicity (DLT)

    (COHORT-1) Dose limiting toxicity (DLT) defined as according to the NCI CTCAE v6. AEs attributable to the study agents (possibly / probably / definitely related) will count towards the toxicity stopping boundaries. These include, but not limited to, neutrophil count decreased, thrombocytopenia, and other non-hematologic AEs

    Measured: 2 months

  2. Number of Treatment related adverse events (AEs)

    (COHORT-1) Number of treatment specific adverse events (AEs) by CTCAE v6.0 (COHORT-2) during dose escalation phase

    Measured: 6 months

  3. Overall response rate (ORR) for COHORT-2

    (COHORT-2) Overall response rate (ORR) defined as CR, PR, or CI by the revised IWG-MRT and ELN criteria after 6 cycles of therapy (each cycle is one month.)

    Measured: 6 months

Secondary outcomes (6)

  1. Overall response rate (ORR) for COHORT 1

    (COHORT-1) Overall response rate (ORR) defined as a CR, PR, or CI by the revised IWG-MRT and ELN criteria after 6 cycles of treatment

    Measured: 6 months

  2. Number of treatment related grade ≥ 3 AEs

    (COHORT-2) AEs and serious adverse events (SAEs), as measured by CTCAE v6.0: Number of grade ≥ 3 AEs using CTCAE v6.0.

    Measured: 6 months

  3. Proportion of participants achieving CI

    Proportion of participants achieving CI at cycle 3 and cycle 6 by IWG-MRT and ELN criteria:

    • Anemia response: per IWG-MRT and ELN criteria with screening hemoglobin < 10 g/dL or transfusion dependency
    • Spleen response: per IWG-MRT and ELN criteria with baseline spleen volume > 450 cm3
    • Symptom benefit: per IWG-MRT and ELN criteria with baseline MFSAF v4.0 TSS ≥ 10

    Measured: 3 months and 6 months

  4. Change in spleen volume

    Spleen volume reduction of ≥35% or ≥25% compared to baseline in patients with baseline spleen volume >450cm^3 at completion of cycle 3 and cycle 6

    Measured: 3 months and 6 months

  5. Participants achieving anemia response

    Anemia response as defined by proposed 2024 IWG-ELN criteria in transfusion-dependent or non-transfusion-dependent patients

    Measured: 6 months

  6. Change in symptom response

    Symptom response as defined by 50% reduction from baseline in MPN-SAF TSS at completion of 3 and 6 cycles and by median change in symptom score.

    Measured: 3 months and 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jul 2026
  2. Study start1 Dec 2026 (estimated)
  3. Primary completion1 Dec 2028 (estimated)
  4. Study completion1 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Sequential
Masking
None (open label)
Enrolment
32 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07734077
Sponsor's protocol ID
STUDY-26-00864
Other IDs
5P01CA108671
Acronym
MPN-RC 129
Status last verified
Jul 2026
First submitted
24 Jul 2026
Last updated
29 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No: The completed dataset is the sole property of the Sponsor-Investigator's institution and should not be exported to third parties, except for authorized representatives of appropriate Health/Regulatory Authorities, without permission from the Sponsor-investigator and their institution.

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Revumenib, Ruxolitinib and FEDRATINIB in people with Myelofibrosis and Post-polycythemia Vera Myelofibrosis, run by John Mascarenhas at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 56 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 29 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Gillian Sanchez ((212) 241-1391, gillian.sanchez@mssm.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Dose limiting toxicity (DLT) (time frame: 2 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07734077.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Jul 2026.

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