Last reviewed · How we verify
NCT05294731
Treatment of Chinese Participants With B-Cell Malignancies With BGB-16673, a Bruton Tyrosine Kinase-Targeted Protein-Degrader
Phase 1, PHASE2 trial testing BGB-16673 in B-cell Malignancy in 146 participants. Currently enrolling.
31 January 2029
Quick facts
| Lead sponsor | BeiGene |
|---|---|
| Phase | Phase 1, PHASE2 |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 146 |
| Start date | 6 May 2022 |
| Primary completion | 31 January 2029 |
| Estimated completion | 31 January 2029 |
| Sites | 29 locations across China |
Drugs / interventions tested
- BGB-16673 — full drug profile →
Conditions studied
- B-cell Malignancy — all drugs for B-cell Malignancy →
- Non-Hodgkin Lymphoma — all drugs for Non-Hodgkin Lymphoma →
- Mantle Cell Lymphoma — all drugs for Mantle Cell Lymphoma →
- Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma — all drugs for Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma →
Sponsor
BeiGene — full company profile →
Who can join
18 and older, any sex, with B-cell Malignancy or Non-Hodgkin Lymphoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study aims to explore the recommended phase 2 dose and evaluate the safety, tolerability and preliminary antitumor activity of BGB-16673 monotherapy at the recommended Phase 2 dose for the selected B-cell malignancy expansion cohorts
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
Targeted protein degradation: advances in drug discovery and clinical practice.
Zhong G, Chang X, Xie W, Zhou X. · · 2024 · cited 112× · PMID 39500878 · DOI 10.1038/s41392-024-02004-x -
Proteolysis-Targeting Chimeras (PROTACs) in Cancer Therapy: Present and Future.
Li R, Liu M, Yang Z, Li J, et al · · 2022 · cited 45× · PMID 36557960 · DOI 10.3390/molecules27248828 -
Protein degradation: expanding the toolbox to restrain cancer drug resistance.
Ming H, Li B, Jiang J, Qin S, et al · · 2023 · cited 42× · PMID 36694209 · DOI 10.1186/s13045-023-01398-5 -
Targeting BTK in B Cell Malignancies: From Mode of Action to Resistance Mechanisms.
Mouhssine S, Maher N, Matti BF, Alwan AF, et al · · 2024 · cited 20× · PMID 38542207 · DOI 10.3390/ijms25063234 -
RIPTACs: A groundbreaking approach to drug discovery.
Ma Z, Bolinger AA, Zhou J. · · 2023 · cited 20× · PMID 37734702 · DOI 10.1016/j.drudis.2023.103774 -
Targeted Protein Degradation: Clinical Advances in the Field of Oncology.
Salama AKAA, Trkulja MV, Casanova E, Uras IZ. · · 2022 · cited 19× · PMID 36499765 · DOI 10.3390/ijms232315440 -
Breaking Bad Proteins-Discovery Approaches and the Road to Clinic for Degraders.
Bouvier C, Lawrence R, Cavallo F, Xolalpa W, et al · · 2024 · cited 14× · PMID 38607017 · DOI 10.3390/cells13070578 -
New Means and Challenges in the Targeting of BTK.
Nawaratne V, Sondhi AK, Abdel-Wahab O, Taylor J. · · 2024 · cited 12× · PMID 38578606 · DOI 10.1158/1078-0432.ccr-23-0409
Verify or expand the search:
- PubMed search for NCT05294731
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of BGB-16673
Trials testing the same drug.
- NCT07508995 — A Phase 2 Trial Of The Bruton Tyrosine Kinase Degrader BGB-16673 In Combination With BCL-2 Inhibitor Sonrotoclax For Pat · Phase 2 · not yet recruiting
- NCT06973187 — A Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Adults With Relapsed/Refractory Ch · Phase 3 · recruiting
- NCT07005713 — A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple-Ascending Doses of BGB- · Phase 1 · active not recruiting
- NCT06970743 — A Study of BGB-16673 Compared to Investigator's Choice in Participants With Relapsed/Refractory Chronic Lymphocytic Leuk · Phase 3 · recruiting
- NCT06846671 — A Study of BGB-16673 Compared to Investigator's Choice in Participants With Chronic Lymphocytic Leukemia or Small Lympho · Phase 3 · recruiting
Other recruiting trials for B-cell Malignancy
Currently open trials in the same condition.
- NCT06634589 — A Study to Investigate Safety and Effectiveness of BGB-16673 in Combination With Other Agents in Participants With Relap · Phase 1, PHASE2 · recruiting
Other BeiGene trials
Trials by the same sponsor.
- NCT07169331 — A Study to Evaluate the Efficacy and Safety of Zanubrutinib in Chinese Adults With Treatment-Naive Waldenström Macroglob · Phase 4 · recruiting
- NCT07100938 — A Study Investigating the Efficacy and Safety of BGB-45035 Versus Placebo in Adults With Moderate to Severe Active Rheum · Phase 2 · active not recruiting
- NCT07005713 — A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple-Ascending Doses of BGB- · Phase 1 · active not recruiting
- NCT06906809 — Effect of Phenytoin or Itraconazole on How BGB-16673 is Absorbed and Removed From the Body in Healthy Participants · Phase 1 · completed
- NCT06803680 — A Study of BGB-B455 in Adults With Advanced or Metastatic Solid Tumors · Phase 1 · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05294731 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by BeiGene
- Last refreshed: 17 April 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05294731.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing