Silevertinib clinical trials
How each study uses silevertinib is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
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Example · made-up studies
Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
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Approvals
The first approval found in each region, with its record
- United States
- Not in FDA's approval records
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
How studies write it
Studies that test it under each name
Studies by the year they started
9 studies that test it; most in 2024 (3)
| Year | Studies |
|---|---|
| 2021 | 1 |
| 2022 | 1 |
| 2023 | 1 |
| 2024 | 3 |
| 2025 | 1 |
| 2026 | 2 |
By phase
A phase 1/2 study counts in both.
What it is tested for
Each study’s main condition, where its own words name it, so a study counts once.
Who runs them
Industry 7 · Other 2
Ryvu Therapeutics SA (5) · Black Diamond Therapeutics, Inc. (2) · Bożenna Dembowska Bagińska (1) · St. Joseph's Hospital and Medical Center, Phoenix (1)
Often tested with
Tested in the same studies.
Related medicines
As reviewed, each with the page that says it.
Coming up
From the study records. Dates are the sponsors’ own estimates and often move.
Reaching primary completion within a year · 2
Studies that test silevertinib.
- Dec 2026RVU120 Rollover StudyPhase 2 · Ryvu Therapeutics SA
- Aug 2027Safety and Efficacy of RVU120 Combined With Venetoclax for Treatment of Relapsed/Refractory AMLPhase 2 · Ryvu Therapeutics SA
Studies
Open first, then newest update. How each study uses silevertinib is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 9
- Study of Silevertinib With Temozolomide for the Treatment of Newly Diagnosed GBM With Unmethylated MGMT and EGFRvIIIRecruitingPhase 2Black Diamond Therapeutics, Inc.NCT07326566Written as silevertinib in combination with temozolomide
- A Phase 0/1 Study of BDTX-1535 in Recurrent High-Grade Glioma (rHGG) and Newly Diagnosed Glioblastoma (nGBM) Participants With EGFR Alterations or FusionsRecruitingEarly Phase 1St. Joseph's Hospital and Medical Center, PhoenixNCT06072586Written as BDTX-1535
- Study of CDK8 Inhibitor RVU120 in Combination With Everolimus in Children With Recurrent or Progressive Group 3 or 4 MedulloblastomaNot yet recruitingPhase 1Bożenna Dembowska BagińskaNCT07865130Written as RVU120
- Safety and Efficacy of RVU120 Combined With Venetoclax for Treatment of Relapsed/Refractory AMLRecruitingPhase 2Ryvu Therapeutics SANCT06191263Written as RVU120
- RVU120 Rollover StudyEnrolling by invitationPhase 2Ryvu Therapeutics SANCT06987058Written as RVU120
- RVU120 (SEL120) in Patients With Relapse/Refractory Metastatic or Advanced Solid TumorsTerminatedPhase 1/2Ryvu Therapeutics SANCT05052255Written as RVU120
- Safety and Efficacy of RVU120 for Treatment of Relapsed/Refractory AMLTerminatedPhase 2Ryvu Therapeutics SANCT06268574Written as RVU120
- RVU120 in Patients With Intermediate or High-risk, Primary or Secondary MyelofibrosisTerminatedPhase 2Ryvu Therapeutics SANCT06397313Written as RVU120
- Phase 1/2 Study of Silevertinib (BDTX-1535) in Patients With Glioblastoma or Non-Small Cell Lung Cancer With EGFR MutationsActive, not recruitingPhase 1/2Black Diamond Therapeutics, Inc.NCT05256290Written as silevertinib (BDTX-1535) monotherapy
Codes
What other systems call silevertinib · ClinicalTrials.gg INT017815
- UNII (FDA) RP9F537KVYSILEVERTINIBConfirmed FDA, Wikidata
- Wikidata Q140529325silevertinibConfirmed FDA, Wikidata
- NCI Thesaurus C187115SilevertinibOne source FDA
| System | Code | Name there | Checked by |
|---|---|---|---|
| UNII (FDA) | RP9F537KVY | SILEVERTINIB | Confirmed FDA, Wikidata |
| Wikidata | Q140529325 | silevertinib | Confirmed FDA, Wikidata |
| NCI Thesaurus | C187115 | Silevertinib | One source FDA |
“Confirmed” means two independent publishers link the code to this drug; “one source”, one does and its name agrees.