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NCT Number: NCT07379125

Therapeutic RSK1 Targeting in Myelofibrosis

This is a phase Ib study evaluating PMD-026, an oral inhibitor of ribosomal protein S6 kinase A1 (RSK1), in participants with myelofibrosis (MF).The dose escalation portion utilizes a standard 3+3 design to evaluate two dose levels with an additional dose de-escalation portion to identify the recommended phase II dose (RP2D); subsequently, an additional 6 patients will be enrolled in the dose expansion portion evaluating the efficacy of PMD-026.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Washington University School of Medicine

St Louis, Missouri, 63110, United States

Location status: Recruiting

Location contact

Amy W Zhou, M.D.

CONTACT

[email protected]

314-362-8814

Amy W Zhou, M.D.

PRINCIPAL_INVESTIGATOR

Feng Gao, Ph.D.

SUB_INVESTIGATOR

Liang Huang, M.D.

SUB_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologically confirmed diagnosis of primary myelofibrosis, post-polycythemia vera myelofibrosis or post-essential thrombocythemia myelofibrosis in chronic phase, according to the 2016 WHO criteria
  • Patients must have had at least 1 prior JAK inhibitor treatment for a minimum of 12 weeks and their disease was determined resistant or refractory, and/or their response was lost or intolerant to treatment.
  • Intermediate-2 or High-risk MF, as defined by the Dynamic International Prognostic Scoring System (DIPSS).
  • Presence of measurable disease as defined by:
  • Splenomegaly defined as estimated spleen volume of ≥450 cm3 by imaging with either MRI, CT or ultrasound, or a palpable spleen >=5 cm from the costal margin.
  • Baseline MFSAF v4.0 Total Symptom Score ≥ 10
  • At least 18 years of age.
  • ECOG performance status ≤ 2.
  • Adequate organ function as defined below:
  • Total bilirubin ≤ 1.5 x IULN (unless the participant has a history of Gilbert's syndrome)
  • AST(SGOT)/ALT(SGPT) ≤ 3.0 x IULN
  • Creatinine clearance ≥ 30 mL/min by Cockcroft-Gault
  • Adequate laboratory parameters:
  • Absolute Neutrophil Count (ANC) ≥ 100/mm^3
  • Platelets ≥50,000/mm^3
  • Blasts ≤ 10% on manual differential
  • The effects of PMD-026 on the developing human fetus are unknown. For this reason, women of childbearing potential and men must agree to use adequate contraception prior to study entry, for the duration of study participation, and for 30 days after completion of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study or should a man suspect he has fathered a child, s/he must inform her treating physician immediately.
  • Ability to understand and willingness to sign an IRB approved written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of study participants.

Exclusion criteria

  • Prior allogeneic or autologous stem cell transplantation within the previous 12 months
  • Prior splenectomy
  • Prior splenic irradiation if < 3 months between last radiation and screening visit.
  • Prior or concurrent malignancy whose natural history has the potential to interfere with the safety or efficacy assessment of the investigational regimen. Patients with prior or concurrent malignancy that does NOT meet that definition are eligible for this trial.
  • Currently receiving any other investigational agents or planning to receive any investigational agents within 28 days before the planned first dose of PMD-026.
  • Currently receiving a JAK inhibitor or planning to receive a JAK inhibitor within 7 days before the planned first dose of PMD-026. In patients with ongoing JAK inhibitor therapy (i.e. ruxolitinib) at screening, it must be tapered over a period of at least 7 days. Patients on a low dose of ruxolitinib (e.g. 5 mg QD) may have a reduced taper period or no taper.
  • Known active disease involving the CNS.
  • QTcF >450 msec for males, >470 msec for females (calculated using Fridericia's formula).
  • A history of hypersensitivity or allergic reactions attributed to compounds of similar chemical or biologic composition to PMD-026 or other agents used in the study.
  • Any major surgery within 28 days prior to the first dose of PMD-026.
  • Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, autoimmune disease, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.
  • Unable to swallow or retain oral medications.
  • Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 35 days of study entry (repeated on C1D1).

Treatment and study plan

PMD-026

Drug

PMD-026 is an oral drug which will be taken every 12 hours on an outpatient basis at the assigned dose every day of each 28-day cycle. Provided by Phoenix Molecular Designs.

Primary outcomes

  1. Number of participants with adverse events

    Time frame: From cycle 1 day 1 through 28 days after last dose (estimated to be 1 year and 28 days)

    Graded per CTCAE v5.0.

  2. Number of participants with dose limiting toxicities (DLTs) based on occurrence of serious treatment-emergent adverse events (Dose Escalation only)

    Time frame: During cycle 1 of treatment (each cycle is 28 days)

    Dose limiting toxicities are defined in the protocol.

  3. Recommended phase II dose (RP2D) (Dose Escalation only)

    Time frame: Completion of cycle 1 (each cycle is 28 days) of all dose-escalation patients (estimated to be 1 year and 28 days)

    The RP2D will be determined based on review of safety and tolerability endpoints in dose escalation.

  4. Changes in spleen size (Dose Expansion and RP2D Cohort in Dose Escalation)

    Time frame: Baseline and after 24 weeks of treatment (estimated to be 24 weeks)

    Measured by ultrasound or other abdominal imaging.

  5. Changes in Myelofibrosis Symptom Assessment Form (MFSAF) v4.0 Total Symptom Score (Dose Expansion and PR2D Cohort in Dose Escalation)

    Time frame: Baseline and after 24 weeks of treatment (estimated to be 24 weeks)

    The MFSAF assesses patient's symptom burden with 7-items that are scored from 0 (Absent) to 10 (Worst Imaginable). The total score can range from 0-70 with the higher score meaning more severe symptoms.

  6. Bone marrow histopathologic response (Dose Expansion and RP2D Cohort in Dose Escalation)

    Time frame: Baseline and after 24 weeks of treatment (estimated to be 24 weeks)

    Bone marrow histopathologic response will be evaluated by the International Working Group for Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) criteria.

  7. Overall response rate (ORR) (Dose Expansion and RP2D Cohort in Dose Escalation)

    Time frame: Baseline and after 24 weeks of treatment (estimated to be 24 weeks)

    Defined as CR (complete remission/response) + PR (partial remission/response) + CI (clinical improvement).

    Responses are defined by the International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) consensus.

Secondary outcomes

  1. Percentage of patients with 35% or greater reduction in spleen volume as determined by ultrasound or other imaging modalities

    Time frame: At 24 weeks and at the end of treatment (estimated to be 1 year)

  2. Percentage of participants with 25% or greater reduction in spleen volume as determined by ultrasound or other imaging modalities

    Time frame: At 24 weeks and at the end of treatment (estimated to be 1 year)

  3. Percentage of patients with a 50% or greater improvement in Myelofibrosis Symptom Assessment Form version 4.0 (MFSAF v4.0) Total Symptom Score

    Time frame: At 24 weeks and at the end of treatment (estimated to be 1 year)

    The MFSAF assesses patient's symptom burden with 7-items that are scored from 0 (Absent) to 10 (Worst Imaginable). The total score can range from 0-70 with the higher score meaning more severe symptoms.

  4. Percentage of patients with a reduction in National Institutes of Health Patient Reported Outcomes Measurement Information System (NIH PROMIS) Short Form v2.0 - Physical Function 8c 7-day scores

    Time frame: At 24 weeks and at the end of treatment (estimated to be 1 year)

    The NIH PROMIS is a tool designed to assess physical function in adults. The tool at 8-items with scoring from 5 to 1. Total score is calculated by adding all scores together. The higher the score typically means better physical function.

  5. Overall response rate (ORR)

    Time frame: At 24 weeks and at the end of treatment (estimated to be 1 year)

    Defined as CR (complete remission/response) + PR (partial remission/response) + CI (clinical improvement).

    Responses are defined by the International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) consensus.

  6. Change in bone marrow fibrosis grading by WHO grading

    Time frame: At 24 weeks and at the end of treatment (estimated to be 1 year)

    The WHO scoring for bone marrow fibrosis is as follows: Grade 0 No fibrosis present, Grade 1 Mild fibrosis with some reticulin fibers present but not significantly affecting hematopoiesis, Grade 2 Moderate fibrosis where reticulin fibers are more prominent and begin to impact blood cell production, and Grade 3 Severe fibrosis characterized by extensive collagen deposition that severely impairs hematopoiesis.

  7. Change in blast percentage in the bone marrow

    Time frame: At 24 weeks and at the end of treatment (estimated to be 1 year)

Study contacts

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

Amy W Zhou, M.D.

CONTACT

[email protected]

314-362-8814

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Collaborators

  • Phoenix Molecular Designs
  • Swim Across America
  • The Foundation for Barnes-Jewish Hospital

Registry information

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jan 30, 2026
Registry last updated
May 22, 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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