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resiquimod

Generic: Resiquimod Sulfate

resiquimod: 5 clinical trials tracked.

resiquimod evidence translation

What we can confirm

5 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about resiquimod, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Clinical Trial Registry Records (5)

A Multicenter, Randomized, Double-Blind, Controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of BDB-001 Injection in Patients With ANCA-Associated Vasculitis

NCT07168161Registry updated 2026-08-13·Phase 3
Recruiting

Primary endpoint: The proportion of patients achieving disease remission assessed by Birmingham Vasculitis Activity Score (BVAS)

InterventionalRandomizedquadruple300 targetStarted 2025-11Completion 2028-0250 sites · ChinaStaidson (Beijing) Biopharmaceuticals Co., Ltd

A Multicenter, Randomized, Open-lable, Parallel-controlled, Phase I/II Trial to Study Efficacy and Safety of Substitution of Glucocorticoid for BDB-001 Injection in Patients With ANCA-associated Vasculitis

NCT05197842Registry updated 2025-08-07·Phase 1/Phase 2
Completed

Primary endpoint: The proportion of patients achieving disease complete remission or partial remission assessed by Birmingham Vasculitis Activity Score (BVAS)

InterventionalRandomizedopen93 enrolledStarted 2022-02Completion 2025-0322 sites · ChinaStaidson (Beijing) Biopharmaceuticals Co., Ltd

A Phase 2, Open-label, Multi-Arm Trial to Evaluate the Efficacy and Safety of BDB001 in the Treatment of Subjects With Advanced Solid Tumors That Have Progressed on Anti-PD-1 or Anti-PD-L1 mAb Treatment

NCT04819373Registry updated 2025-11-12·Phase 2·EIKN
Completed

Primary endpoint: Efficacy as measured by Objective Response Rate

Interventionalopen1 enrolledStarted 2021-08Completion 2023-051 site · United StatesEikon Therapeutics

Phase 1 Open-Label Dose Escalation Study of BDB001 as a Single Agent and in Combination With Atezolizumab in Subjects With Advanced Solid Tumors

NCT04196530Registry updated 2025-11-12·Phase 1·EIKN
Completed

Primary endpoint: Safety and Tolerability: incidence of adverse events and any dose limiting toxicity

Interventionalopen40 enrolledStarted 2019-11Completion 2024-085 sites · United StatesEikon Therapeutics

Phase 1 Open-Label Dose Escalation Study of BDB001 as a Single Agent and in Combination With Pembrolizumab in Subjects With Advanced Solid Tumors

NCT03486301Registry updated 2025-11-12·Phase 1·EIKN
Completed

Primary endpoint: Safety and Tolerability: incidence of adverse events and any dose limiting toxicity

Interventionalopen87 enrolledStarted 2018-02Completion 2024-045 sites · United StatesEikon Therapeutics