About this trial

Evaluation of BL-M07D1 for injection in Phase I clinical study of safety, tolerability, pharmacokinetic Characteristics, and initial efficacy in patients with locally advanced or metastatic digestive tract tumors and other solid tumors.

Eligibility criteria

Qualifiers

Sign informed consent voluntarily and follow protocol requirements.

No gender limitation.

Age: ≥18 years and ≤75 years (phase Ia); ≥18 years old (phase Ib).

The expected survival time is ≥3 months.

Disqualifiers

Antitumor therapy such as chemotherapy, biotherapy, immunotherapy, radical radiotherapy, major surgery, targeted therapy (including small-molecule tyrosine kinase inhibitors) within 4 weeks prior to initial administration or within 5 half-lives, whichever is shorter; Mitomycin and nitrosourea were administered within 6 weeks before the first administration. Oral fluorouracil drugs such as Tizio, capecitabine, or palliative radiotherapy within 2 weeks prior to initial administration; Traditional Chinese medicines or proprietary Chinese medicines with anti-tumor indications should be administered within 2 weeks before the first administration.

Previously received ADC drug therapy with camptothecin derivatives (topoisomerase I inhibitors) as toxins (Phase Ib only).

History of severe heart disease, such as symptomatic congestive heart failure (CHF) ≥2 (CTCAE 5.0), New York Heart Society (NYHA) ≥2 heart failure, history of transmural myocardial infarction, unstable angina, etc.

Prolonged QT interval (QTcF > 450 msec in men or 470 msec in women), complete left bundle branch block, and degree III atrioventricular block.

Trial design

Treatments tested in this trial

  • BL-M07D1

Treatment groups

26 Participants
are divided into 1 treatment group

Locations

1
Fudan University ShangHai Cancer Center200100, ShanghaiShanghai Municipality, China

Sponsors and collaborators

Sichuan Baili Pharmaceutical Co., Ltd.

Lead sponsor

SystImmune Inc.

Collaborator

Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.

Collaborator