A Study of BL-M11D1 in Patients With Relapsed/Refractory Myelodysplastic Syndromes
A Phase Ib/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Efficacy of BL-M11D1 for Injection in Patients With Relapsed/Refractory Myelodysplastic Syndromes
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Contact
Study Contact
- Name: Sa Xiao, PHD
- Phone Number: 15013238943
- Email: xiaosa@baili-pharm.com
Study Locations
-
-
Tianjin Municipality
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Tianjin, Tianjin Municipality, China
- Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences
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Contact:
- Zhijian Xiao
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-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Voluntarily sign the informed consent form and comply with the protocol requirements;
- No gender restrictions;
- Age: ≥18 years and ≤75 years;
- Expected survival time ≥3 months;
- Relapsed/refractory CD33+ MDS;
- Morphological assessment showing blasts in bone marrow ≥5% and <20%;
- Eastern Cooperative Oncology Group (ECOG) performance status ≤2;
- Toxicities from prior anti-tumor therapy must have recovered to ≤ Grade 1 as defined by NCI-CTCAE v6.0;
- Meet the required organ function levels;
- For premenopausal women of childbearing potential, a pregnancy test (serum/urine) must be negative within 7 days before starting treatment, and they must not be breastfeeding; all enrolled trial participants (regardless of gender) must practice adequate barrier contraception throughout the entire treatment period and for 6 months after treatment completion.
Exclusion Criteria:
- Use of chemotherapy, biotherapy, immunotherapy, etc., within 4 weeks or 5 half-lives prior to the first dose;
- Presence of uncorrected folate deficiency or vitamin B12 deficiency, etc.;
- History of severe cardiovascular or cerebrovascular disease;
- Thromboembolic events requiring therapeutic intervention within 6 months prior to screening;
- Active autoimmune diseases and inflammatory diseases;
- History of extensive bowel resection or presence of Crohn's disease, ulcerative colitis, chronic diarrhea, or intestinal obstruction;
- Diagnosis of another malignancy within 5 years prior to the first dose;
- Poorly controlled hypertension;
- Poorly controlled hyperglycemia or diabetes mellitus;
- Pulmonary diseases classified as Grade ≥3 according to CTCAE v6.0, etc.;
- Trial participants with central nervous system involvement;
- Trial participants with extramedullary involvement;
- Trial participants with a history of allergy to recombinant humanized antibodies or chimeric human-mouse antibodies, or hypersensitivity to any excipient component of BL-M11D1;
- Prior organ transplantation or hematopoietic stem cell transplantation;
- Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
- Active fungal, bacterial, or viral infections;
- History of severe neurological or psychiatric disorders;
- Trial participants with clinically significant bleeding or obvious bleeding tendency within 4 weeks prior to signing informed consent;
- Presence of clinically symptomatic pleural, peritoneal, or pericardial effusion requiring repeated drainage;
- Participation in another clinical trial within 4 weeks or 5 half-lives prior to the first dose;
- Pregnant or breastfeeding women;
- Other conditions deemed by the investigator to make the participant unsuitable for participation in this clinical trial.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: BL-M11D1
Participants receive BL-M11D1 for the first cycle (4 weeks).
Participants with clinical benefit could receive additional treatment for more cycles.
The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
|
Administration by intravenous infusion for a cycle of 4 weeks.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Phase II: Objective Response Rate (ORR)
Time Frame: Up to approximately 24 months
|
ORR is defined as the percentage of participants, who has a CR (disappearance of all target lesions) or PR (at least a 30% decrease in the sum of diameters of target lesions).
The percentage of participants who experiences a confirmed CR or PR is according to RECIST 1.1.
|
Up to approximately 24 months
|
|
Phase Ib: Recommended Phase II Dose (RP2D)
Time Frame: Up to approximately 24 months
|
The RP2D is defined as the dose level chosen by the sponsor (in consultation with the investigators) for phase II study, based on safety, tolerability, efficacy, PK, and PD data collected during the dose escalation study of BL-M11D1.
|
Up to approximately 24 months
|
|
Phase Ib: Treatment-Emergent Adverse Event (TEAE)
Time Frame: Up to approximately 24 months
|
TEAE is defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally emerging, or any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a pre-existing condition during the treatment of BL-M11D1.
The type, frequency and severity of TEAE will be evaluated during the treatment of BL-M11D1.
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Up to approximately 24 months
|
|
Phase II: Complete Response (CR)
Time Frame: Up to approximately 24 months
|
Complete Response (CR) is defined as the disappearance of all target lesions, with any pathological lymph nodes (whether target or non-target) having a short axis diameter reduced to <10 mm.
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Up to approximately 24 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
AUC0-t
Time Frame: Up to approximately 24 months
|
AUC0-t is defined as area under the serum concentration-time curve from time 0 to the time of the last measurable concentration.
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Up to approximately 24 months
|
|
Cmax
Time Frame: Up to approximately 24 months
|
Maximum serum concentration (Cmax) of BL-M11D1 will be investigated.
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Up to approximately 24 months
|
|
Tmax
Time Frame: Up to approximately 24 months
|
Time to maximum serum concentration (Tmax) of BL-M11D1 will be investigated.
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Up to approximately 24 months
|
|
Ctrough
Time Frame: Up to approximately 24 months
|
Ctrough is defined as the lowest serum concentration of BL-M11D1 prior to the next dose will be administered.
|
Up to approximately 24 months
|
|
ADA (anti-drug antibody)
Time Frame: Up to approximately 24 months
|
Frequency of anti-BL-M11D1 antibody (ADA) will be investigated.
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Up to approximately 24 months
|
|
T1/2
Time Frame: Up to approximately 24 months
|
Half-life (T1/2) of BL-M11D1 will be investigated.
|
Up to approximately 24 months
|
|
CL (Clearance)
Time Frame: Up to approximately 24 months
|
CL in the serum of BL-M11D1 per unit of time will be investigated.
|
Up to approximately 24 months
|
|
Phase II: Duration of Response (DOR)
Time Frame: Up to approximately 24 months
|
The DOR for a responder is defined as the time from the participant's initial objective response to the first date of either disease progression or death, whichever occurs first.
|
Up to approximately 24 months
|
|
Phase II: Hematologic Improvement (HI)
Time Frame: Up to approximately 24 months
|
HI is defined as achieving a predefined threshold of improvement in the erythroid, platelet, or neutrophil lineages according to the IWG 2006 and IWG 2023 criteria, with a duration of no less than 8 weeks.
|
Up to approximately 24 months
|
|
Phase II: AML Transformation Rate
Time Frame: Up to approximately 24 months
|
The AML transformation rate is defined as the first confirmed event of transformation to acute myeloid leukemia according to WHO criteria (bone marrow blasts ≥20% or presence of extramedullary infiltration).
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Up to approximately 24 months
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- BL-M11D1-102
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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