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Phase 2

Development Phase

1

Upcoming Catalysts

0

Historical Events

1

Regulatory Approvals

Upcoming Catalysts
What are catalysts?
Nov '26
ONCPhase 2

Zanubrutinib Phase 2 Est. Readout

Zanubrutinib
Nov 2026~
CT.gov
00%
Competitive Landscape

1 competitor in Chronic Lymphocytic Leukemia

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Drug Information

Target Indication

Chronic Lymphocytic Leukemia

Clinical Trial

NCT06637501

Last updated: 1/10/2026

Patent & Exclusivity

No patent data available. Pre-approval drugs may not have Orange Book listings.

Regulatory Approvals
EMA11/22/2021

Brukinsa

Brukinsa as monotherapy is indicated for the treatment of adult patients with Waldenström’s macroglobulinaemia (WM) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. Brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (MZL) who have received at least one prior anti-CD20-based therapy. Brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL). Brukinsa in combination with obinutuzumab is indicated for the treatment of adult patients with refractory or relapsed follicular lymphoma (FL) who have received at least two prior systemic therapies.

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Drug Science
Mechanism of action & safety profile
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