Acalabrutinib
Phase 1/2ActiveDevelopment Stage
Phase I: Relapsed or Refractory B-cell Malignancies
Phase I: Relapsed or Refractory B-cell Malignancies, Phase II Cohort A: Relapsed or Refractory Mantle Cell Lymphoma, Phase II Cohort B: Relapsed or Refractory Chronic Lymphocytic Leukemia
Apr 29, 2020 → Jun 24, 2026
About Acalabrutinib
Acalabrutinib is a phase 1/2 stage product being developed by AstraZeneca for Phase I: Relapsed or Refractory B-cell Malignancies. The current trial status is active. This product is registered under clinical trial identifier NCT03932331. Target conditions include Phase I: Relapsed or Refractory B-cell Malignancies, Phase II Cohort A: Relapsed or Refractory Mantle Cell Lymphoma, Phase II Cohort B: Relapsed or Refractory Chronic Lymphocytic Leukemia.
Hype Score Breakdown
Clinical Trials (15)
| NCT ID | Phase | Status |
|---|---|---|
| NCT06757647 | Phase 2 | Recruiting |
| NCT06651970 | Approved | Recruiting |
| NCT06205498 | Pre-clinical | Active |
| NCT05256641 | Phase 1/2 | Recruiting |
| NCT05557695 | Pre-clinical | Recruiting |
| NCT04660045 | Phase 2 | Withdrawn |
| NCT05038904 | Phase 2 | Completed |
| NCT04198922 | Phase 2 | Active |
| NCT04548648 | Phase 2 | Active |
| NCT04497948 | Phase 1 | Terminated |
| NCT04380688 | Phase 2 | Completed |
| NCT04346199 | Phase 2 | Completed |
| NCT03932331 | Phase 1/2 | Active |
| NCT04008706 | Phase 3 | Completed |
| NCT03968848 | Phase 1 | Completed |
Competing Products
20 competing products in Phase I: Relapsed or Refractory B-cell Malignancies
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| TERN-701 | Terns Pharmaceuticals | Phase 1/2 | 38 |
| Tamsulosin HCl + Solifenacin Succinate + EC905 | Astellas Pharma | Phase 1 | 33 |
| solifenacin succinate + mirabegron + mirabegron/solifenacin succinate | Astellas Pharma | Phase 1 | 33 |
| Graceptor® | Astellas Pharma | Pre-clinical | 23 |
| Lemborexant + Placebo | Eisai | Approved | 85 |
| BIW-8962 | Kyowa Kirin | Phase 1/2 | 41 |
| Sacituzumab tirumotecan | Merck | Phase 2 | 52 |
| progesterone + Progesterone | Merck | Approved | 85 |
| Asciminib | Novartis | Pre-clinical | 23 |
| Nilotinib | Novartis | Phase 3 | 77 |
| Imatinib mesylate | Novartis | Phase 3 | 77 |
| Imatinib Mesylate 600 MG Oral Tablet + Imatinib Mesylate 400 MG Oral Tablet + Imatinib Mesylate | Novartis | Phase 3 | 77 |
| ribociclib + Trametinib | Novartis | Phase 1 | 33 |
| Nilotinib | Novartis | Approved | 85 |
| Imatinib | Novartis | Phase 3 | 77 |
| Nilotinib | Novartis | Approved | 85 |
| Gleevec | Novartis | Phase 2 | 52 |
| Nilotinib + Ruxolitinib | Novartis | Phase 1/2 | 41 |
| ABL001 | Novartis | Phase 3 | 77 |
| asciminib | Novartis | Phase 2 | 52 |