A Study of SGN-B6A in Chinese Participants With Advanced Solid Tumors
Sponsored by Seagen Inc.
About this trial
Last updated 9 months ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Started 10 months ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
- Subjects must have histologically or cytologically confirmed metastatic or unresectable locally advanced solid malignancy within one of the tumor types listed below.
- Subjects must have disease that is relapsed or refractory, or be intolerant to systemic standard-of-care therapies, and in the judgement of the investigator, should have no appropriate standard-of-care therapeutic option. If a standard-of-care therapy is available that has not been administered, the reason that the therapy is not appropriate must be documented.
- Adequate organ function as defined by the baseline laboratory criteria obtained within 7 days prior to SGN-B6A initiation (Cycle 1 Day 1)
- Measurable or non-measurable disease per RECIST v1.1 at baseline.
- An Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1.
Exclusion Criteria
- History of another malignancy within 3 years before the first dose of study intervention, or any evidence of residual disease from a previously diagnosed malignancy. Exceptions are malignancies with a negligible risk of metastasis or death.
- Participants with any of the following respiratory conditions:
- Pre-existing peripheral neuropathy Grade greater than or equal to (≥) 2
- Uncontrolled diabetes mellitus
- Known active central nervous system metastases. Participants with previously treated brain metastases may participate provided they:
- Known history or current diagnosis of carcinomatous meningitis
- Previous treatment with an MMAE-containing agent or an agent targeting integrin beta-6
- Prior anticancer therapies:
- Traditional or herbal medicines: