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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 developer

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 · 2 study sponsors
Clinical Trials (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

NCT07168161·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

NCT05197842·Phase 1/Phase 2·EIGR
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

NCT04819373·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

NCT04196530·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

NCT03486301·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