- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Acalabrutinib.
Displaying page 1 of 3.
EudraCT Number: 2015-003213-18 | Sponsor Protocol Number: RHMCAN1129 | Start Date*: 2017-01-13 | |||||||||||
Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
Full Title: A Phase Ib/II combination trial of acalabrutinib with rituximab, cyclophosphamide, doxorubicin,vincristine and prednisolone (R-CHOP) for patients with diffuse large B-cell lymphoma (DLBCL) | |||||||||||||
Medical condition: Diffuse large B-cell lymphomas (most common type of non-Hodgkins lymphoma) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006081-36 | Sponsor Protocol Number: FILOCLL14-STAIR | Start Date*: 2021-08-11 |
Sponsor Name:FILO | ||
Full Title: STop and restart Acalabrutinib In fRail patients with previously untreated CLL (STAIR) | ||
Medical condition: Chronic lymphoid leukemia | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005220-26 | Sponsor Protocol Number: ACE-LY-308 | Start Date*: 2017-05-16 | |||||||||||
Sponsor Name:Acerta Pharma BV | |||||||||||||
Full Title: A Phase 3, Randomized, Double blind, Placebo controlled, Multicenter Study of Bendamustine and Rituximab (BR) alone Versus in Combination with Acalabrutinib (ACP 196) in Subjects with Previously Un... | |||||||||||||
Medical condition: Mantle Cell Lymphoma | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) GR (Ongoing) PL (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001642-18 | Sponsor Protocol Number: D8230C00002 | Start Date*: 2021-05-13 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Modular Phase I/II, Open-label, Multicentre Study to Assess AZD4573 in Novel Combinations with Anti-cancer Agents in Patients with Advanced Haematological Malignancies | |||||||||||||
Medical condition: Haematological Malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) ES (Temporarily Halted) FR (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004396-38 | Sponsor Protocol Number: IELSG49 | Start Date*: 2021-06-07 | |||||||||||
Sponsor Name:IELSG - International Extranodal Lymphoma Study Group | |||||||||||||
Full Title: Phase II trial of acalabrutinib in combination with tafasitamab in patients with previously treated marginal zone lymphomas (MZL) | |||||||||||||
Medical condition: Marginal Zone Lymphomas refractory to or in first or greater relapse after prior systemic therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000111-84 | Sponsor Protocol Number: ACE-LY-003 | Start Date*: 2020-02-04 | |||||||||||||||||||||
Sponsor Name:ACERTA PHARMA BV | |||||||||||||||||||||||
Full Title: An Open-label, Phase 1b/2 Study of Acalabrutinib Alone or in Combination Therapy in Subjects with B-cell Non-Hodgkin Lymphoma | |||||||||||||||||||||||
Medical condition: B-cell Non-Hodgkin Lymphoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001644-25 | Sponsor Protocol Number: ACE-ID-201/D822FC00001 | Start Date*: 2020-05-06 | |||||||||||
Sponsor Name:Acerta Pharma B.V. | |||||||||||||
Full Title: A Phase 2 Randomized Study of the Efficacy and Safety of Acalabrutinib with Best Supportive Care Versus Best Supportive Care in Subjects Hospitalized with COVID-19 | |||||||||||||
Medical condition: Subjects with life-threatening COVID-19 symptoms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005317-68 | Sponsor Protocol Number: ACE-CL-208 | Start Date*: 2016-05-16 | |||||||||||
Sponsor Name:Acerta Pharma B.V. | |||||||||||||
Full Title: A Phase 2 Study of the Efficacy and Safety of ACP-196 in Subjects with Relapsed/Refractory CLL and Intolerant of Ibrutinib Therapy | |||||||||||||
Medical condition: High Risk Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003737-15 | Sponsor Protocol Number: ACE-CL-110 | Start Date*: 2017-10-16 | |||||||||||
Sponsor Name:Acerta Pharma BV | |||||||||||||
Full Title: A Phase 1/2 Proof-of-Concept Study Investigating AZD6738 monotherapy and Acalabrutinib in Combination with AZD6738 (ATR inhibitor) in Subjects with Relapsed or Refractory High-risk Chronic Lymphocy... | |||||||||||||
Medical condition: Relapsed or Refractory High-risk Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001804-39 | Sponsor Protocol Number: GLLC-EARLY | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name:Fundación PETHEMA | |||||||||||||
Full Title: Phase III Randomized Study to Investigate the Use of Acalabrutinib in the Treatment of Patients With Early Stage CLL With High Risk of Early Disease Progression | |||||||||||||
Medical condition: Early Stage CLL With High Risk of Early Disease Progression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002464-31 | Sponsor Protocol Number: KRT-232-111 | Start Date*: 2021-02-12 | |||||||||||||||||||||
Sponsor Name:Kartos Therapeutics Inc. | |||||||||||||||||||||||
Full Title: An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of KRT-232 in Combination with Acalabrutinib in Subjects with Relapsed/Refractory Diffuse Large B-cell Lymphoma or Relapsed/R... | |||||||||||||||||||||||
Medical condition: - Relapsed/Refractory (R/R) de novo TP53 ABC (non-GCB) or GCB diffuse large B-cell lymphoma (DLBCL) - R/R TP53 chronic lymphocytic leukemia (CLL) naïve to prior Bruton's tyrosine kinase (BTK) inhib... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Completed) PT (Completed) FR (Completed) BE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003876-42 | Sponsor Protocol Number: SAKK38/19 | Start Date*: 2022-04-29 | |||||||||||
Sponsor Name:SAKK | |||||||||||||
Full Title: Assessing a ctDNA and PET-oriented therapy in patients with DLBCL. A multicenter, open-label, phase II trial | |||||||||||||
Medical condition: Disseminated large B cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004454-17 | Sponsor Protocol Number: ACE-CL-309 | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:Acerta Pharma BV | |||||||||||||
Full Title: A Randomized, Multicenter, Open-Label, Phase 3 Study of Acalabrutinib (ACP-196) Versus Investigator’s Choice of Either Idelalisib Plus Rituximab or Bendamustine Plus Rituximab in Subjects with Rela... | |||||||||||||
Medical condition: Relapsed or Refractory Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Trial now transitioned) SK (Completed) SE (Completed) ES (Ongoing) CZ (Trial now transitioned) AT (Completed) DE (Completed) FR (Completed) BG (Completed) PL (Trial now transitioned) HR (Trial now transitioned) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002443-28 | Sponsor Protocol Number: ACE-CL-311/D8221C00001 | Start Date*: 2019-05-08 | |||||||||||
Sponsor Name:Acerta Pharma B.V. | |||||||||||||
Full Title: A Randomized, Multicenter, Open-Label, Phase 3 Study to Compare the Efficacy and Safety of Acalabrutinib (ACP-196) in Combination with Venetoclax with and without Obinutuzumab Compared to Investiga... | |||||||||||||
Medical condition: Previously untreated Chronic Lymphocytic Leukemia Without del(17p) or TP53 Mutation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Restarted) HU (Ongoing) CZ (Ongoing) SK (Trial now transitioned) PL (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) DK (Trial now transitioned) SE (Trial now transitioned) BG (Ongoing) NL (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004401-40 | Sponsor Protocol Number: RG_17-194 | Start Date*: 2019-01-31 | ||||||||||||||||
Sponsor Name:University of Birmingham | ||||||||||||||||||
Full Title: STELLAR: A phase II, randomiSed study of CHOP-R in combination with acalabruTinib comparEd to CHOP-R in patients with newLy diagnosed Richter’s Syndrome (RS) and a pLAtfoRm for initial investigatio... | ||||||||||||||||||
Medical condition: Richter's Syndrome | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002142-17 | Sponsor Protocol Number: CLL-Frail | Start Date*: 2021-11-24 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: CLL-Frail – A prospective, multicenter phase II trial of acalabrutinib in very old (≥80y) or frail CLL-Patients | |||||||||||||
Medical condition: Patients with CLL requiring treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003212-36 | Sponsor Protocol Number: ACE-WM-001 | Start Date*: 2014-12-09 | ||||||||||||||||
Sponsor Name:Acerta Pharma BV | ||||||||||||||||||
Full Title: An Open-label, Phase 1b/2 Study of ACP-196 in Subjects with Waldenström Macroglobulinemia | ||||||||||||||||||
Medical condition: Waldenström Macroglobulinemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) FR (Trial now transitioned) GR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003736-21 | Sponsor Protocol Number: ACE-LY-110 | Start Date*: 2017-06-07 | ||||||||||||||||
Sponsor Name:Acerta Pharma BV | ||||||||||||||||||
Full Title: A Phase 1/2 Proof-of-Concept Study of the Combination of Acalabrutinib and Vistusertib in Subjects with Relapsed/Refractory B-cell Malignancies | ||||||||||||||||||
Medical condition: Part 1: De novo Diffuse large B-cell lymphoma (DLBCL), Transformed DLBCL and Richter syndrome (RS). Part 2: De novo Germinal center B-cell (GCB) DLBCL and De novo non-GCB DLBCL | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004360-26 | Sponsor Protocol Number: CLL16 | Start Date*: 2021-08-24 |
Sponsor Name:German CLL Study Group (University of Cologne) | ||
Full Title: A PROSPECTIVE, OPEN-LABEL, MULTICENTER, RANDOMIZED, PHASE 3 TRIAL OF ACALABRUTINIB, OBINUTUZUMAB AND VENETOCLAX (GAVE) COMPARED TO OBINUTUZUMAB AND VENETOCLAX (GVE) IN PREVIOUSLY UNTREATED PATIENTS... | ||
Medical condition: Patients with previously untreated chronic lymphocytic leukemia with treatment requiring disease and at least one out of three risk factors (17p-deletion, TP53 mutation or Complex karyotype). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001755-39 | Sponsor Protocol Number: ACE-LY-312(D8227C00001) | Start Date*: 2020-11-30 | |||||||||||
Sponsor Name:Acerta Pharma B.V. (A Member of the AstraZeneca Group) | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Acalabrutinib in Combination with Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Subjects ≤75 Yea... | |||||||||||||
Medical condition: Diffuse large B-cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) AT (Ongoing) PT (Trial now transitioned) BE (Trial now transitioned) CZ (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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