Study of BMF-219 in Healthy Adult Subjects and in Adult Subjects With Type 2 Diabetes Mellitus (T2D)
- Summary
- A Phase 1/ 2 Randomized, Double-Blind, Placebo-Controlled Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BMF-219, an Oral Covalent Menin Inhibitor, in Healthy Adult Subjects and in Adult Subjects with Type 2 Diabetes Mellitus.
- Short title
- Study of BMF-219 in Healthy Adult Subjects and in Adult Subjects With Type 2 Diabetes Mellitus (T2D)
- Official title
- A Phase 1/2 Randomized, Double-Blind, Placebo-Controlled Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, PK, and PD of BMF-219, an Oral Covalent Menin Inhibitor, in Healthy Adults and Adults With T2D
- Registry reports results
- Listing at source
- Listed
- Recruitment status
- Completed
- Phase
- Phase 1/Phase 2
- Study type
- Interventional
- Completion date
- 2025-07-08
- First posted
- 2023-02-16
- Registry last updated
- 2025-11-10
- Primary completion date
- 2024-11-18
- Start date
- 2022-08-17
- Actual participants
- Participants
- Participant count basis
- Actual
- Protocol amendments
- Number of sites
- Data monitoring committee
- Registry sponsor category
- Industry
- Lead sponsor
- Biomea Fusion Inc.
- Source registry
- ClinicalTrials.gov
- Registry ID
- NCT05731544
- ClinicalTrials.gov ID
- NCT05731544
- Registry record
- Open registry record
- Allocation
- Randomised
- Model
- Parallel groups
- Purpose
- Treatment
- Masking
- Double masking
- Masking description
- The subject and the investigator involved in the treatment or clinical evaluation of the subjects will be unaware of the group assignments.
- Masked roles
- Participants, Investigators
Safety Assessments
Timeframe: 52 weeks
Assessed by treatment emergent adverse events. (TEAEs), drug discontinuation due to TEAEs, serious adverse events, clinically significant laboratory, vital, and ECG evaluations.
Pharmacokinetics Assessments
Timeframe: 12 weeks
Assessed by effect of fed conditions on serial and sparse pharmacokinetic data.
Change in HbA1c
Timeframe: 26 weeks
Assess the change in HbA1c from baseline to week 26.
To assess the effect on HbA1c
Timeframe: 26 Weeks
Proportion of subjects achieving an HbA1c \< 7% at Week 26.
- Sex
- All
- Age groups
- Adults, Older adults
- Minimum age
- 18 Years
- Maximum age
- 65 Years
- Healthy volunteers
- Yes
Healthy Subject Inclusion Criteria:
- Males or females, age ≥18 and ≤65 years.
- BMI ≥18 and ≤35 kg/m2.
- Subjects are healthy on the basis of their medical history, physical examination, ECG, and routine laboratory data.
- All subjects must be willing and able to provide written, signed informed consent and be willing and able to comply with all study procedures and tests.
Subjects with T2D: (MAD Cohorts) Inclusion Criteria:
- Males or females, age ≥18 and ≤65 years.
- Diagnosed with T2D within the last 15 years.
- Treated with lifestyle management with or without at the most 3 anti-diabetic medications with a stable dose for at least 2 months prior to screening. If on metformin, the stable dose should be at least 500mg/day.
- HbA1c ≥7.0% and ≤10.5%.
- BMI ≥25 and ≤40 kg/m2.
- Females are to be not pregnant, non-lactating.
- All Subjects must be willing and able to provide written, signed informed consent and be willing and able to comply with all study procedures and tests.
Subjects with T2D: (Expansion Cohort) Inclusion Criteria:
- Males or females, age ≥18 and ≤65 years.
- Diagnosed with T2D within the last 7 years.
- Treated with lifestyle management with or without at the most 3 anti-diabetic medications with a stable dose for at least 2 months prior to screening. If on metformin, the stable dose should be at least 500mg/day.
- HbA1c ≥7.0% and ≤10.5%.
- BMI ≥25 and ≤40 kg/m2.
- Females are to be not pregnant, non-lactating.
- All Subjects must be willing and able to provide written, signed informed consent and be willing and able to comply with all study procedures and tests.
Healthy Subject Exclusion Criteria:
- Evidence or history of any clinically significant disease or malignancy.
- Mean QTcF ≥ 440 msec on triplicate ECGs. Use of medications known to significantly prolong the QT or QTcF interval.
- History of hypertension or untreated hypertension (sitting systolic blood pressure (BP) ≥140 and diastolic BP ≥90 mm Hg).
- Known self or family history (first-degree relative) of multiple endocrine neoplasia Type 1.
- History of stomach or intestinal surgery or resection (except appendectomy, hernia repair, and/or cholecystectomy).
- A history or evidence of HIV, HCV, or HBV infection at screening or active COVID-19 infection on screening.
- Receiving an investigational intervention or having participated in another clinical trial within 30 days.
- Currently dieting (formal weight loss program) and/or are currently using or have used within 2 months of screening any drugs for weight management.
- Received prior menin inhibitor treatment.
Subjects with T2D (MAD Cohorts) Exclusion Criteria:
- Type 1 Diabetes Mellitus or a secondary form of diabetes or any prior history of diabetic ketoacidosis.
- Have had recurrence (≥2 episodes) of severe hypoglycemia (defined by the occurrence of neuroglycopenic symptoms requiring the assistance of another person for recovery) within the last 6 months prior to screening or, has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms as judged by the Investigator.
- Known self or family history (first-degree relative) of multiple endocrine neoplasia Type 1.
- Use of anti-diabetes medications (sulfonylureas, insulin, dipeptidyl peptidase-IV inhibitor [DPP-4I] [linagliptin and saxagliptin only] thiazolidinediones) within last 2 months prior to screening.
- Fasting plasma glucose ≥255 mg/dL, fasting C-peptide <0.8 ng/mL, fasting insulin >55 μIU/mL.
- Mean QTcF ≥450 ms. Use of medications known to significantly prolong the QT or QTc interval.
- Fasting triglyceride ≥500 mg/dL.
- Have an eGFR <60 mL/min/1.73 Equation at screening.
- AST or ALT > 1.5 × ULN, bilirubin > 1.5 × ULN. Isolated GGT elevation >2.5 ULN without > 1.5 x ULN AST, ALT and/or total bilirubin but with a history of abnormal LFTs in the last 6 months or a medical history of a liver disorder should be excluded.
- History of acute or chronic pancreatitis and serum lipase and/or amylase above 1.5 x ULN.
- Active HBV or active HCV at screening. Known positive test, if any, prior to screening or history of HIV. An active COVID-19 infection at screening.
- TSH >6 mIU/L or <0.4 mIU/L (on stable thyroid replacement dose for 3 months prior to screening).
- Severe uncontrolled treated or untreated hypertension (systolic blood pressure >150 mmHg or diastolic blood pressure >90 mmHg).
- History of stomach or intestinal surgery or resection and/or gastroparesis (except that appendectomy, hernia repair, and/or cholecystectomy will be allowed).
- History of cirrhosis.
- Currently dieting (formal weight loss program) and/or are currently using or have used within 2 months of screening any drugs for weight management.
Subjects with T2D (Expansion Cohort) Exclusion Criteria:
- Type 1 Diabetes Mellitus or a secondary form of diabetes.
- Prior history of diabetic ketoacidosis or hyperosmolar coma.
- History of severe hypoglycemia (defined by the occurrence of neuroglycopenic symptoms requiring the assistance of another person for recovery) within the last 6 months prior to screening or, has a history of hypoglycemia unawareness.
- Known self or family history (first-degree relative) of multiple endocrine neoplasia Type 1 (MEN1).
- Use of any of the following anti-diabetes medications within 2 months prior to screening: sulfonylureas, insulin, and the dipeptidyl peptidase-4 inhibitors (DPP4i) linagliptin and saxagliptin (sitagliptin and other DPP4i allowed) thiazolidinones [TZD]) within last 2 months prior to screening.
- Fasting plasma glucose ≥255 mg/dL, fasting C-peptide <0.8 ng/mL, fasting insulin >55 μIU/mL.
- Mean QTcF interval >450 ms on triplicate ECGs. Use of prescription or over-the-counter medications known to significantly prolong the QT or QTc interval is excluded.
- Fasting triglyceride ≥500 mg/dL.
- eGFR<60 mL/min/1.73.
- AST or ALT >1.5 × ULN, Total bilirubin >1.5 × ULN at screening.
- History of acute or chronic pancreatitis and serum lipase and/or amylase above 1.5 x ULN.
- Active HBV or active HCV at screening. Known positive test or history of HIV. An active COVID-19 infection at screening.
- TSH >6 mIU/L or <0.4 mIU/L (on stable thyroid replacement dose for 3 months prior to screening).
- Severe uncontrolled treated or untreated hypertension (systolic blood pressure >150 mmHg or diastolic blood pressure >90 mmHg).
- History of stomach or intestinal surgery or resection and/or gastroparesis.
- History of cirrhosis.
- Currently dieting (formal weight loss program) and/or are currently using or have used within 2 months of screening any drugs for weight management.
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Related records
Drugs (1)
Lead sponsors (1)
Conditions (2)
- Diabetes mellitus
- Type 2 diabetes mellitus Primary condition