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CompletedNCT03136185Updated Jan 10, 2024Results posted

Bomedemstat (IMG-7289/MK-3543) in Participants With Myelofibrosis (IMG-7289-CTP-102/MK-3543-002)

A Phase 1/2 interventional study of Bomedemstat in Myelofibrosis, Post-polycythemia Vera Myelofibrosis (PPV-MF) and Post-essential Thrombocythemia Myelofibrosis (PET-MF), sponsored by Imago BioSciences, Inc., a subsidiary of Merck & Co., Inc., (Rahway, New Jersey USA). Completed at 5 sites in 5 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-01-10.

Sponsored by Imago BioSciences, Inc., a subsidiary of Merck & Co., Inc., (Rahway, New Jersey USA) · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
90
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This is a Phase 1/2 open-label study to evaluate the safety, tolerability, steady-state pharmacokinetic (PK) and pharmacodynamics (PD) of a lysine-specific demethylase 1 (LSD1) inhibitor, bomedemstat (IMG-7289/MK-3543), administered orally once daily in participants with myelofibrosis.

The primary hypothesis is that bomedemstat is a safe and tolerable orally available agent when administered to participants with myelofibrosis including primary myelofibrosis (PMF), post-polycythaemia vera-myelofibrosis (PPVMF), and post-essential thrombocythaemia-myelofibrosis (PET-MF) (collectively referred to as 'MF'); inhibition of LSD1 by bomedemstat will reduce spleen size in those with splenomegaly, improve haematopoiesis and reduce constitutional symptoms associated with these disorders.

Read the detailed description

This study initiated as a Phase 1/2a study assessing the safety of the starting dose, an 85-day duration of treatment, and the PK and PD effects of bomedemstat, with transition to a Phase 2b study incorporating changes supported by the Phase 1/2a data.

02

Conditions studied

  • Myelofibrosis
  • Post-polycythemia Vera Myelofibrosis (PPV-MF)
  • Post-essential Thrombocythemia Myelofibrosis (PET-MF)
  • Primary Myelofibrosis (PMF)

Keywords

  • LSD1
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • >18 years of age
  • Diagnosis of either PMF per World Health Organization (WHO) diagnostic criteria for myeloproliferative neoplasms, or PPV-MF or PET-MF per the International Working Group for Myelofibrosis Research and Treatment
  • High or intermediate-2 risk disease

Exclusion criteria

Exclusion Criteria:

  • Receiving other treatments for the condition (with exceptions and time limits)
  • Major surgery in last 4 weeks, any surgery in the last 2 weeks
  • History of, or scheduled, hematopoietic stem cell transplant within 24 weeks of Screening
  • History of splenectomy
  • Current use of prohibited medications
  • A concurrent second active and nonstable malignancy
  • Known human immunodeficiency virus infection or active Hepatitis B or Hepatitis C virus infection
  • Other hematologic/biochemistry requirements, as per protocol
  • Use of an investigational agent within last 14 days
  • Pregnant or lactating females
04

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
90 participants (actual)

Study arms

  • Experimental
    Ph 1/2a PMF: Bomedemstat 0.25 mg/kg/d

    In the Phase 1/2a portion of the study, PMF participants received 0.25 mg/kg/d bomedemstat orally every day (qd) for 85 days during the Initial Treatment Period (ITP). Qualifying participants could continue to receive treatment for an additional 85 days during an Additional Treatment Period (ATP) as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/d

    In the Phase 1/2a portion of the study, PPV-MF participants received 0.25 mg/kg/d bomedemstat orally qd for 85 days during the ITP. Qualifying participants could continue to receive treatment for an additional 85 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 1/2a PET-MF: Bomedemstat 0.25 mg/kg/d

    In the Phase 1/2a portion of the study, PET-MF participants received 0.25 mg/kg/d bomedemstat orally qd for 85 days during the ITP. Qualifying participants could continue to receive treatment for an additional 85 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 2b PMF: Bomedemstat 0.5 mg/kg/d

    In the Phase 2b portion of the study, PMF participants received 0.5 mg/kg/d bomedemstat orally qd for 169 days during the ITP. Qualifying participants could continue to receive treatment for an additional 169 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 2b PPV-MF: Bomedemstat 0.5 mg/kg/d

    In the Phase 2b portion of the study, PPV-MF participants received 0.5 mg/kg/d bomedemstat orally qd for 169 days during the ITP. Qualifying participants could continue to receive treatment for an additional 169 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 2b PET-MF: Bomedemstat 0.5 mg/kg/d

    In the Phase 2b portion of the study, PET-MF participants received 0.5 mg/kg/d bomedemstat orally qd for 169 days during the ITP. Qualifying participants could continue to receive treatment for an additional 169 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 2b PMF: Bomedemstat 0.6 mg/kg/d

    In the Phase 2b portion of the study, PMF participants received 0.6 mg/kg/d bomedemstat orally qd for 169 days during the ITP. Qualifying participants could continue to receive treatment for an additional 169 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 2b PPV-MF: Bomedemstat 0.6 mg/kg/d

    In the Phase 2b portion of the study, PPV-MF participants received 0.6 mg/kg/d bomedemstat orally qd for 169 days during the ITP. Qualifying participants could continue to receive treatment for an additional 169 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

  • Experimental
    Ph 2b PET-MF: Bomedemstat 0.6 mg/kg/d

    In the Phase 2b portion of the study, PET-MF participants received 0.6 mg/kg/d bomedemstat orally qd for 169 days during the ITP. Qualifying participants could continue to receive treatment for an additional 169 days during an ATP as determined by the investigator. The ATP could repeat indefinitely in participants that continued to derive clinical benefit.

    Drug: Bomedemstat

Interventions

  • DrugBomedemstat

    Oral (capsule) administration according to dose allocation.

    Also known as: IMG-7289, MK-3543, LSD1 inhibitor

05

What researchers measure

Primary outcomes

  1. Number of Participants With Dose Limiting Toxicities (DLTs)

    DLT was defined as any one of the following adverse events (AEs) that occured through Day 7 of the Initial Treatment Period (ITP) and was considered by the Investigator to be possibly, probably or definitely related to bomedemstat: * Thrombocytopenia leading to clinically significant sequelae (i.e., a clinically significant bleeding event or the need for prophylactic transfusions) * A clinically significant bleeding event in a participant with a platelet count \>50 x 10\^9/L (50 k/μL) * Any Grade 4 or 5 non-haematologic adverse event * Any Grade 3 non-haematologic adverse event with failure to recover to Grade 2 within 7 days of drug cessation, with the following exceptions: ≥ Grade 3 nausea, vomiting or diarrhea that responds to standard medical care; ≥ Grade 3 aesthenia lasting less than 14 days; any Grade 3 electrolyte abnormality unrelated to the underlying malignancy and persisting greater than 24 hours. The number of participants with a DLT were reported.

    Time frame: Up to Day 7 of the ITP

  2. Number of Participants With Serious Adverse Events

    An AE was any undesirable physical, psychological or behavioral effect experienced by a participant, in conjunction with the use of the drug or biologic, whether or not product-related. This included any untoward signs or symptoms experienced by the participant from the time of first dose with bomedemstat until completion of the study. Serious AEs (SAEs) were any AE that resulted in death, life-threatening experience, required or prolonged inpatient hospitalization, persistent or significant disability/incapacity, congenital anomaly, or important medical events. The number of participants with at least one treatment-emergent (TE) SAE was reported for each arm.

    Time frame: Up to approximately 30 months

  3. Number of Participants With Adverse Events

    An AE was any undesirable physical, psychological or behavioral effect experienced by a participant, in conjunction with the use of the drug or biologic, whether or not product-related. This included any untoward signs or symptoms experienced by the participant from the time of first dose with bomedemstat until completion of the study. The number of participants with at least one TE AE was reported for each arm.

    Time frame: Up to approximately 30 months

  4. Number of Participants That Discontinued Study Treatment Due To AEs

    An AE was any undesirable physical, psychological or behavioral effect experienced by a participant, in conjunction with the use of the drug or biologic, whether or not product-related. This included any untoward signs or symptoms experienced by the participant from the time of first dose with bomedemstat until completion of the study. The number of participants that discontinued study treatment with bomedemstat due to a TE AE was reported for each arm.

    Time frame: Up to approximately 29 months

  5. Phase 1/2a Portion: Observed Maximum Concentration (Cmax) of Bomedemstat

    Cmax was defined as the maximum observed concentration after administration obtained directly from the concentration time profile. Blood and plasma samples were collected at pre-specified timepoints to calculate Cmax in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

    Time frame: Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.

  6. Phase 1/2a Portion: Time to Maximum Concentration (Tmax) of Bomedemstat

    Tmax was defined as the time to maximum concentration after administration obtained by inspection. Blood and plasma samples were collected at pre-specified timepoints to calculate Tmax in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

    Time frame: Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.

  7. Phase 1/2a Portion: Area Under the Concentration-time Curve of Bomedemstat From Time 0 to 24 Hours Post-dose (AUC0-24)

    AUC0-24 was defined as the area under the concentration versus time curve calculated using the linear trapezoidal rule from the zero time-point to the 24-hour time-point concentration. Blood and plasma samples were collected at pre-specified timepoints to calculate AUC0-24 in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

    Time frame: Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.

  8. Phase 1/2a Portion: Apparent Total Clearance (CL/F) of Bomedemstat After Oral Administration

    CL/F was defined as the apparent total clearance of drug after oral administration. Blood and plasma samples were collected at pre-specified timepoints to calculate CL/F in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

    Time frame: Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.

  9. Percentage Change From Baseline in Spleen Volume

    Change in spleen volume was assessed based on calculated spleen volume (ml) measured by magnetic resonance imaging (MRI), or computerized tomography (CT) scan (where locally permitted) if the participant was not a candidate for MRI from Day 0. Percentage change from baseline in spleen volume was reported at Initial Treatment Period (ITP) Day 84, ITP Day 168, Additional Treatment Period 1 (ATP1) Day 84 (Study Day 253), and ATP1 Day 168 (Study Day 337).

    Time frame: Baseline, ITP Day 84 (Study Day 84), ITP Day 168 (Study Day 168), ATP1 Day 84 (Study Day 253), and ATP1 Day 168 (Study Day 337)

  10. Percentage Change From Baseline in Spleen Size

    Change in spleen size was assessed based on spleen palpation (in cm) at each visit. Percentage change from baseline in spleen size was reported at ITP Day 84, ITP Day 168, ATP1 Day 84 (Study Day 253), ATP1 Day 168 (Study Day 337), ATP2 Day 84 (Study Day 422), ATP2 Day 168 (Study Day 506), and ATP3 Day 84 (Study Day 591). As prespecified by the Statistical Analysis Plan, assessments for the Phase 1/2 groups were summarized using visit windowing after the Day 84 visit of the ITP to allow for comparison with the Phase 2b groups at ITP Day 168.

    Time frame: Baseline, ITP Day 84 (Study Day 84), ITP Day 168 (Study Day 168), ATP1 Day 84 (Study Day 253), ATP1 Day 168 (Study Day 337), ATP2 Day 84 (Study Day 422), ATP2 Day 168 (Study Day 506), and ATP3 Day 84 (Study Day 591)

06

Results

Posted Jan 10, 2024

Participant flow

Participants with primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (PPV-MF), and post-essential thrombocythemia myelofibrosis (PET-MF) were recruited for this study.

Participant flow — Overall Study
MilestonePh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Started9368511241113
Treated9368511241113
Entered additional treatment period (atp)6233141759
Completed initial treatment period (itp)73441418810
Completed1002031457
Not completed8366581066
Withdrew: Adverse event013122511
Withdrew: Death000110100
Withdrew: Physician decision311212101
Withdrew: Protocol defined disease progression001001011
Withdrew: Withdrawal by subject101111233
Withdrew: Not reported410102110

Outcome measures

PrimaryNumber of Participants With Dose Limiting Toxicities (DLTs)

DLT was defined as any one of the following adverse events (AEs) that occured through Day 7 of the Initial Treatment Period (ITP) and was considered by the Investigator to be possibly, probably or definitely related to bomedemstat: * Thrombocytopenia leading to clinically significant sequelae (i.e., a clinically significant bleeding event or the need for prophylactic transfusions) * A clinically significant bleeding event in a participant with a platelet count \>50 x 10\^9/L (50 k/μL) * Any Grade 4 or 5 non-haematologic adverse event * Any Grade 3 non-haematologic adverse event with failure to recover to Grade 2 within 7 days of drug cessation, with the following exceptions: ≥ Grade 3 nausea, vomiting or diarrhea that responds to standard medical care; ≥ Grade 3 aesthenia lasting less than 14 days; any Grade 3 electrolyte abnormality unrelated to the underlying malignancy and persisting greater than 24 hours. The number of participants with a DLT were reported.

Time frame:
Up to Day 7 of the ITP
Reported as:
Count of participants · Participants
Number of Participants With Dose Limiting Toxicities (DLTs)
ParticipantsPh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Number of Participants With Dose Limiting Toxicities (DLTs)000000000
PrimaryNumber of Participants With Serious Adverse Events

An AE was any undesirable physical, psychological or behavioral effect experienced by a participant, in conjunction with the use of the drug or biologic, whether or not product-related. This included any untoward signs or symptoms experienced by the participant from the time of first dose with bomedemstat until completion of the study. Serious AEs (SAEs) were any AE that resulted in death, life-threatening experience, required or prolonged inpatient hospitalization, persistent or significant disability/incapacity, congenital anomaly, or important medical events. The number of participants with at least one treatment-emergent (TE) SAE was reported for each arm.

Time frame:
Up to approximately 30 months
Reported as:
Count of participants · Participants
Number of Participants With Serious Adverse Events
ParticipantsPh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Number of Participants With Serious Adverse Events4254471233
PrimaryNumber of Participants With Adverse Events

An AE was any undesirable physical, psychological or behavioral effect experienced by a participant, in conjunction with the use of the drug or biologic, whether or not product-related. This included any untoward signs or symptoms experienced by the participant from the time of first dose with bomedemstat until completion of the study. The number of participants with at least one TE AE was reported for each arm.

Time frame:
Up to approximately 30 months
Reported as:
Count of participants · Participants
Number of Participants With Adverse Events
ParticipantsPh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Number of Participants With Adverse Events9368511231012
PrimaryNumber of Participants That Discontinued Study Treatment Due To AEs

An AE was any undesirable physical, psychological or behavioral effect experienced by a participant, in conjunction with the use of the drug or biologic, whether or not product-related. This included any untoward signs or symptoms experienced by the participant from the time of first dose with bomedemstat until completion of the study. The number of participants that discontinued study treatment with bomedemstat due to a TE AE was reported for each arm.

Time frame:
Up to approximately 29 months
Reported as:
Count of participants · Participants
Number of Participants That Discontinued Study Treatment Due To AEs
ParticipantsPh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Number of Participants That Discontinued Study Treatment Due To AEs015124523
PrimaryPhase 1/2a Portion: Observed Maximum Concentration (Cmax) of Bomedemstat

Cmax was defined as the maximum observed concentration after administration obtained directly from the concentration time profile. Blood and plasma samples were collected at pre-specified timepoints to calculate Cmax in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

Time frame:
Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.
Reported as:
Geometric mean · ng/mL
Phase 1/2a Portion: Observed Maximum Concentration (Cmax) of Bomedemstat
ng/mLPh 1/2a Portion: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Plasma12.63 ± 104.41——————
Blood26.27 ± 66.76——————
PrimaryPhase 1/2a Portion: Time to Maximum Concentration (Tmax) of Bomedemstat

Tmax was defined as the time to maximum concentration after administration obtained by inspection. Blood and plasma samples were collected at pre-specified timepoints to calculate Tmax in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

Time frame:
Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.
Reported as:
Median · hour
Phase 1/2a Portion: Time to Maximum Concentration (Tmax) of Bomedemstat
hourPh 1/2a Portion: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Plasma1.00 (0.50 to 2.85)——————
Blood1.05 (0.50 to 3.02)——————
PrimaryPhase 1/2a Portion: Area Under the Concentration-time Curve of Bomedemstat From Time 0 to 24 Hours Post-dose (AUC0-24)

AUC0-24 was defined as the area under the concentration versus time curve calculated using the linear trapezoidal rule from the zero time-point to the 24-hour time-point concentration. Blood and plasma samples were collected at pre-specified timepoints to calculate AUC0-24 in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

Time frame:
Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.
Reported as:
Geometric mean · hour•ng/mL
Phase 1/2a Portion: Area Under the Concentration-time Curve of Bomedemstat From Time 0 to 24 Hours Post-dose (AUC0-24)
hour•ng/mLPh 1/2a Portion: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Plasma63.90 ± 68.56——————
Blood265.92 ± 68.92——————
PrimaryPhase 1/2a Portion: Apparent Total Clearance (CL/F) of Bomedemstat After Oral Administration

CL/F was defined as the apparent total clearance of drug after oral administration. Blood and plasma samples were collected at pre-specified timepoints to calculate CL/F in participants of the Phase 1/2a portion of the study. As pre-specified by the protocol and Pharmacokinetic Analysis Plan (PAP), Phase 2b participants were excluded from this analysis.

Time frame:
Day 21: Pre-dose and 0.5, 1, 2, 3, 4, 8, and 24 hours (Day 22) after dosing.
Reported as:
Geometric mean · mL/min
Phase 1/2a Portion: Apparent Total Clearance (CL/F) of Bomedemstat After Oral Administration
mL/minPh 1/2a Portion: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Plasma12787.43 ± 63.72——————
Blood3067.57 ± 85.78——————
PrimaryPercentage Change From Baseline in Spleen Volume

Change in spleen volume was assessed based on calculated spleen volume (ml) measured by magnetic resonance imaging (MRI), or computerized tomography (CT) scan (where locally permitted) if the participant was not a candidate for MRI from Day 0. Percentage change from baseline in spleen volume was reported at Initial Treatment Period (ITP) Day 84, ITP Day 168, Additional Treatment Period 1 (ATP1) Day 84 (Study Day 253), and ATP1 Day 168 (Study Day 337).

Time frame:
Baseline, ITP Day 84 (Study Day 84), ITP Day 168 (Study Day 168), ATP1 Day 84 (Study Day 253), and ATP1 Day 168 (Study Day 337)
Reported as:
Mean · Percentage Change
Percentage Change From Baseline in Spleen Volume
Percentage ChangePh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
ITP Day 84 (Study Day 84)3.3 (-50.5 to 57.0)-13.7 (-49.6 to 22.2)2.2 (-110.3 to 114.8)-9.1 (-27.9 to 9.6)-7.2 (-80.2 to 65.8)0.3 (-32.3 to 32.9)10.0 (1.2 to 18.8)-2.3 (-31.5 to 26.9)1.2 (-10.9 to 13.2)
ITP Day 168 (Study Day 168)———-23.9 (-43.2 to -4.6)-19.6 (NA to NA)-33.7 (-43.8 to -23.6)12.3 (-4.1 to 28.6)-15.4 (-56.7 to 25.8)-4.4 (-20.6 to 11.8)
ATP1 Day 84 (Study Day 253)—————-27.7 (NA to NA)———
ATP1 Day 168 (Study Day 337)———-36.5 (NA to NA)—-38.9 (NA to NA)37.4 (-55.6 to 130.5)6.0 (-302.0 to 313.9)-15.0 (-39.0 to 9.0)
PrimaryPercentage Change From Baseline in Spleen Size

Change in spleen size was assessed based on spleen palpation (in cm) at each visit. Percentage change from baseline in spleen size was reported at ITP Day 84, ITP Day 168, ATP1 Day 84 (Study Day 253), ATP1 Day 168 (Study Day 337), ATP2 Day 84 (Study Day 422), ATP2 Day 168 (Study Day 506), and ATP3 Day 84 (Study Day 591). As prespecified by the Statistical Analysis Plan, assessments for the Phase 1/2 groups were summarized using visit windowing after the Day 84 visit of the ITP to allow for comparison with the Phase 2b groups at ITP Day 168.

Time frame:
Baseline, ITP Day 84 (Study Day 84), ITP Day 168 (Study Day 168), ATP1 Day 84 (Study Day 253), ATP1 Day 168 (Study Day 337), ATP2 Day 84 (Study Day 422), ATP2 Day 168 (Study Day 506), and ATP3 Day 84 (Study Day 591)
Reported as:
Mean · Percentage Change
Percentage Change From Baseline in Spleen Size
Percentage ChangePh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
ITP Day 84 (Study Day 84)-36.5 (-68.0 to -5.0)9.6 (-95.1 to 114.2)24.1 (-79.4 to 127.7)20.7 (-132.2 to 173.7)-28.1 (-257.8 to 201.6)11.0 (-70.7 to 92.7)-34.7 (-58.1 to -11.3)-38.2 (-53.4 to -23.1)-59.6 (-113.4 to -5.7)
ITP Day 168 (Study Day 168)-20.7 (-48.3 to 6.9)-39.6 (NA to NA)116.3 (-1794.8 to 2027.4)-27.8 (NA to NA)—-36.1 (-212.6 to 140.4)-24.8 (-74.2 to 24.5)-28.5 (-60.1 to 3.0)-41.2 (-102.9 to 20.6)
ATP1 Day 84 (Study Day 253)———-27.8 (NA to NA)—-36.1 (-212.6 to 140.4)-27.9 (-84.8 to 29.0)-50.4 (-101.7 to 0.9)-28.4 (-97.7 to 40.9)
ATP1 Day 168 (Study Day 337)-19.0 (NA to NA)——-27.8 (NA to NA)—-38.9 (-180.1 to 102.3)-1.9 (-151.0 to 147.3)-38.9 (NA to NA)-82.4 (-117.4 to -47.4)
ATP2 Day 84 (Study Day 422)-4.8 (NA to NA)————-37.5 (-196.3 to 121.3)—-44.4 (NA to NA)—
ATP2 Day 168 (Study Day 506)—————-22.0 (NA to NA)———
ATP3 Day 84 (Study Day 591)—————-11.1 (-152.3 to 130.1)———

Adverse events

Collected over Up to approximately 30 months. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Ph 1/2a PMF: Bomedemstat 0.25 mg/kg/d0/9 (0%)4/9 (44.4%)9/9 (100%)
Ph 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/d0/3 (0%)2/3 (66.7%)3/3 (100%)
Ph 1/2a PET-MF: Bomedemstat 0.25 mg/kg/d0/6 (0%)5/6 (83.3%)6/6 (100%)
Ph 2b PMF: Bomedemstat 0.5 mg/kg/d1/8 (12.5%)4/8 (50%)8/8 (100%)
Ph 2b PPV-MF: Bomedemstat 0.5 mg/kg/d1/5 (20%)4/5 (80%)5/5 (100%)
Ph 2b PET-MF: Bomedemstat 0.5 mg/kg/d0/11 (0%)7/11 (63.6%)11/11 (100%)
Ph 2b PMF: Bomedemstat 0.6 mg/kg/d1/24 (4.2%)12/24 (50%)23/24 (95.8%)
Ph 2b PPV-MF: Bomedemstat 0.6 mg/kg/d0/11 (0%)3/11 (27.3%)10/11 (90.9%)
Ph 2b PET-MF: Bomedemstat 0.6 mg/kg/d0/13 (0%)3/13 (23.1%)12/13 (92.3%)
Most frequent serious events
Showing 10 of 65
Most frequent serious events
EventPh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
Abdominal painGastrointestinal disorders0/92/32/60/81/52/111/241/111/13
NauseaGastrointestinal disorders0/92/33/62/81/52/114/241/111/13
ThrombocytopeniaBlood and lymphatic system disorders2/91/33/64/82/57/111/243/113/13
AnaemiaBlood and lymphatic system disorders2/90/33/62/82/55/112/242/112/13
GoutMetabolism and nutrition disorders0/90/33/60/80/51/111/240/110/13
ArthralgiaMusculoskeletal and connective tissue disorders2/91/33/60/82/52/113/241/110/13
Oedema peripheralGeneral disorders2/90/31/64/82/51/111/241/111/13
HeadacheNervous system disorders1/90/31/61/82/50/111/240/110/13
PneumoniaInfections and infestations0/90/30/63/80/52/111/240/111/13
Abdominal discomfortGastrointestinal disorders0/91/31/60/80/51/112/240/110/13
Most frequent other events
Showing 10 of 291
Most frequent other events
EventPh 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/d
ThrombocytopeniaBlood and lymphatic system disorders5/92/34/67/83/58/114/246/114/13
AnaemiaBlood and lymphatic system disorders7/92/35/62/83/55/115/243/113/13
DiarrhoeaGastrointestinal disorders4/91/35/63/80/54/119/242/112/13
NauseaGastrointestinal disorders0/92/33/65/82/53/117/243/112/13
Upper respiratory tract infectionInfections and infestations1/92/31/61/80/50/110/240/110/13
Weight decreasedInvestigations1/92/31/61/82/51/111/240/112/13
ArthralgiaMusculoskeletal and connective tissue disorders4/92/33/60/82/52/115/243/111/13
DizzinessNervous system disorders1/92/31/60/81/51/111/242/110/13
DysgeusiaNervous system disorders6/92/33/63/80/54/116/243/115/13
EpistaxisRespiratory, thoracic and mediastinal disorders0/92/32/62/80/51/112/241/112/13

Baseline characteristics

Age, Continuous
Age, Continuous(Years)Ph 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/dTotal
Mean62.6 ± 12.4374.7 ± 5.5164.7 ± 6.5969.6 ± 8.3864.8 ± 7.4669.4 ± 14.4065.2 ± 9.4266.7 ± 9.2761.3 ± 12.0765.7 ± 10.51
Sex: Female, Male
Sex: Female, Male(Participants)Ph 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/dTotal
Female104446128443
Male832415123947
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Ph 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/dTotal
Hispanic or Latino0010011003
Not Hispanic or Latino83584102211980
Unknown or Not Reported1000101047
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Ph 1/2a PMF: Bomedemstat 0.25 mg/kg/dPh 1/2a PPV-MF: Bomedemstat 0.25 mg/kg/dPh 1/2a PET-MF: Bomedemstat 0.25 mg/kg/dPh 2b PMF: Bomedemstat 0.5 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.5 mg/kg/dPh 2b PET-MF: Bomedemstat 0.5 mg/kg/dPh 2b PMF: Bomedemstat 0.6 mg/kg/dPh 2b PPV-MF: Bomedemstat 0.6 mg/kg/dPh 2b PET-MF: Bomedemstat 0.6 mg/kg/dTotal
American Indian or Alaska Native0000000000
Asian000010105521
Black or African American0000010012
Native Hawaiian or Other Pacific Islander0000001001
White726749126659
Other1100000002
Multiple0000000011
Not Reported1001011004
07

Study locations

5 sites
  • University of Michigan
    Ann Arbor, Michigan 48105, United States
  • Royal Adelaide Hospital
    Adelaide, South Australia, Australia
  • Universitatsklinikum Essen
    Essen, 45147, Germany
  • Azienda Ospedaliero Universitaria Careggi
    Florence, Italy
  • Guy's and St Thomas' Hospitals
    London, United Kingdom
08

References and documents

Study documents

  • Study protocol · Jun 23, 2020
  • Statistical analysis plan · Nov 18, 2021

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — http://engagezone.msd.com/doc/ProcedureAccessClinicalTrialData.pdf

09

Registry details

Key details

Study ID
NCT03136185
Lead sponsor
Imago BioSciences, Inc., a subsidiary of Merck & Co., Inc., (Rahway, New Jersey USA)
Responsible party
Sponsor
First posted
May 2, 2017
Start date
Jul 18, 2017
Primary completion
Mar 8, 2022
Completion
Mar 8, 2022
Results posted
Jan 10, 2024
Last update
Jan 10, 2024

Study contacts

Medical Director
study director · Merck Sharp & Dohme LLC

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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