Phase Ib: Explore the safety and tolerability of BL-M07D1 to further define RP2D in a variety of solid tumors, including locally advanced or metastatic urinary and gastrointestinal tumors. Phase II: To explore the efficacy of BL-M07D1 in patients with a variety of solid tumors including locally advanced or metastatic HER2-positive/low-expressing urinary and gastrointestinal tumors.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
42
BL-M07D1 was administered by intravenous infusion every 3 weeks in 3-week cycles.
Cancer Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
RECRUITINGPhase Ib: Recommended Phase II Dose (RP2D)
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.
Time frame: Up to approximately 24 months
Phase II: Objective response rate (ORR)
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.
Time frame: Up to approximately 24 months
Phase Ib/II: Treatment-Emergent Adverse Event (TEAE)
TEAE is defined as any adverse and unexpected change in body structure, function, or chemistry or any exacerbation of an existing condition (i.e., any clinically significant adverse change in frequency and/or intensity) during treatment. The type, frequency, and severity of TEAE will be assessed during treatment.
Time frame: Up to approximately 24 months
Phase Ib: Objective response rate (ORR)
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.
Time frame: Up to approximately 24 months
Phase Ib/II: Disease control rate (DCR)
The DCR is defined as the percentage of participants who has a CR, PR, or Stable Disease (SD: neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease \[PD: at least a 20% increase in the sum of diameters of target lesions and an absolute increase of at least 5 mm. The appearance of one or more new lesions is also considered PD\]).
Time frame: Up to approximately 24 months
Phase Ib/II: Duration of response (DOR)
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.
Time frame: Up to approximately 24 months
Phase II: Progression-free survival (PFS)
The PFS is defined as the time from the first dose of medication to disease progression or death, whichever occurred first.
Time frame: Up to approximately 24 months
Phase Ib/II: Cmax
Maximum serum concentration (Cmax) of BL-M07D1 will be investigated.
Time frame: Up to approximately 24 months
Phase Ib/II: Tmax
Time to maximum serum concentration (Tmax) of BL-M07D1 will be investigated.
Time frame: Up to approximately 24 months
Phase Ib: T1/2
Half-life (T1/2) of BL-M07D1 will be investigated.
Time frame: Up to approximately 24 months
Phase Ib: AUC0-t
Blood concentration - Area under time line.
Time frame: Up to approximately 24 months
Phase Ib: CL
The serum clearance rate of BL-M07D1 per unit time will be investigated.
Time frame: Up to approximately 24 months
Phase Ib/II: Ctrough
Ctrough is defined as the lowest serum concentration of BL-M07D1 prior to the next dose will be administered.
Time frame: Up to approximately 24 months
Phase Ib/II: Anti-drug antibody (ADA)
Frequency and titer of anti-BL-M07D1 antibody (ADA) will be evaluated.
Time frame: Up to approximately 24 months
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