Safety, Tolerability and Pharmacokinetics of a Monoclonal Antibody Specific to B-and T-Lymphocyte Attenuator (BTLA) as Monotherapy and in Combination With an Anti-PD1 Monoclonal Antibody for Injection in Subjects With Advanced Malignancies
A First-in-Human, Multicenter, Open-Label, Phase 1 Dose-Escalation and Cohort Expansion Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TAB004 as Monotherapy and in Combination With Toripalimabin Subjects With Advanced Solid Malignancies Including Lymphoma
Sponsor: CTI Clinical Trial and Consulting Services
This PHASE1 trial investigates Advanced Unresectable Solid Tumor and Metastatic Solid Tumor and is currently actively recruiting participants. CTI Clinical Trial and Consulting Services leads this study, which shows 17 recorded versions since 2019 — indicating substantial longitudinal coverage. As an oncology study, it adds to the longitudinal record of treatment development for this indication.
Status Flow
Change History
17 versions recorded-
Sep 2025 — Present [monthly]
Recruiting PHASE1
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Sep 2024 — Sep 2025 [monthly]
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Jul 2024 — Sep 2024 [monthly]
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Mar 2024 — Jul 2024 [monthly]
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Jun 2023 — Mar 2024 [monthly]
Recruiting PHASE1
▶ Show 12 earlier versions
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Mar 2023 — Jun 2023 [monthly]
Recruiting PHASE1
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Jul 2022 — Mar 2023 [monthly]
Recruiting PHASE1
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Jun 2022 — Jul 2022 [monthly]
Recruiting PHASE1
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Jan 2022 — Jun 2022 [monthly]
Recruiting PHASE1
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Sep 2021 — Jan 2022 [monthly]
Recruiting PHASE1
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May 2021 — Sep 2021 [monthly]
Recruiting PHASE1
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Jan 2021 — May 2021 [monthly]
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Dec 2020 — Jan 2021 [monthly]
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Jul 2020 — Dec 2020 [monthly]
Recruiting PHASE1
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Mar 2020 — Jul 2020 [monthly]
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Dec 2019 — Mar 2020 [monthly]
Recruiting PHASE1
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Nov 2019 — Dec 2019 [monthly]
Recruiting PHASE1
First recorded
Oct 2019
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- CTI Clinical Trial and Consulting Services
- Shanghai Junshi Bioscience Co., Ltd.
- TopAlliance Biosciences
For direct contact, visit the study record on ClinicalTrials.gov .