BR is named as an intervention in 4 current clinical trials in our USA, UK, China and India registers. 1 is recruiting patients now. The most common phase is Phase 2/3. The sponsor with the most trials is Gilead Sciences (1). The most-studied condition is Acquired Immune Deficiency Syndrome (AIDS).
| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
A Study of Surovatamig (AZD0486) Plus Rituximab in Previously Untreated Follicular Lymphoma Patients
NCT06549595 · ClinicalTrials.gov ↗ · Untreated Follicular Lymphoma
|
Phase 3 | Recruiting | AstraZeneca | UK, USA, India, China |
|
BR Combined With OR in Treatment-naïve Marginal Zone Lymphoma
NCT07008053 · ClinicalTrials.gov ↗ · Marginal Zone Lymphomas
|
Phase 2 | Not yet open | Tianjin Medical University Cancer Institute and Hospital | China |
|
Study of Cobicistat-Boosted Atazanavir (ATV/co), Cobicistat-Boosted Darunavir (DRV/co) and Emtricitabine/Tenofovir Alafenamide (F/TAF) in Children With HIV
NCT02016924 · ClinicalTrials.gov ↗ · Acquired Immune Deficiency Syndrome (AIDS), HIV Infections
|
Phase 2/3 | Active, closed | Gilead Sciences | UK, USA |
|
A Study of Acalabrutinib in Combination With Rituximab + (Bendamustine or Venetoclax) in Subjects With MCL
NCT02717624 · ClinicalTrials.gov ↗ · Mantle Cell Lymphoma (MCL)
|
Phase 1 | Active, closed | Acerta Pharma BV | USA |
Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.
| Lead sponsor | Trials |
|---|---|
| Gilead Sciences | 1 |
| AstraZeneca | 1 |
| Acerta Pharma BV | 1 |
| Tianjin Medical University Cancer Institute and Hospital | 1 |
| Register | Trials | Recruiting |
|---|---|---|
| Clinical trials in USA | 3 | 1 |
| Clinical trials in UK | 2 | 1 |
| Clinical trials in China | 2 | 1 |
| Clinical trials in India | 1 | 1 |
A trial with sites in more than one country appears in each of those registers.
4 current trials in our USA, UK, China and India registers name BR as a drug or biological intervention, as of the registry sync on 25 September 2026. Completed and withdrawn studies are not counted.
Yes. 1 of the 4 trials is recruiting: 1 with sites in USA, 1 with sites in UK, 1 with sites in China and 1 with sites in India. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Gilead Sciences (1), AstraZeneca (1), Acerta Pharma BV (1) and Tianjin Medical University Cancer Institute and Hospital (1). The number in brackets is how many trials each organisation leads.
Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how BR works or whether it is effective, and it is not medical advice.
Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how BR works or whether it is effective. Each trial links to its own record so you can check it yourself.
This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists BR (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 25 Sep 2026.