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Drugs in development · updated 13 November 2026

Birelentinib: clinical trials and development status

Other names and codes: DZD8586

FDA substance registryNot approved in the USNo EMA authorisationEstimated US launch Mar 2030 – Jan 2031 (Phuturdex estimate)

As of 13 November 2026 Birelentinib is in 7 active clinical trials (recruiting or ongoing, phases I–III) for 3 diseases. The most advanced phase is III.

Authorisation

Sources: EMA, AIFA register (open data), FDA. For Germany only the EU centralised authorisation is shown: the national BfArM register is not one of our sources.

Where Birelentinib trials are recruiting

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7Active trials
IIIMost advanced phase
3Diseases studied

What it is

An orally bioavailable non-covalent dual inhibitor of tyrosine-protein kinases Lyn (LYN) and BTK (Bruton's tyrosine kinase; Bruton agammaglobulinemia tyrosine kinase), with potential antineoplastic activity. Upon oral administration, birelentinib targets and inhibits both LYN and BTK, thereby blocking both BTK-dependent and BTK-independent B-cell antigen receptor (BCR) signaling pathways. This prevents the proliferation of malignant B-cells in which the BCR signaling pathway is overactivated. Birelentinib is able to cross the blood-brain barrier (BBB) and thus potentially useful in the treatment of central nervous system (CNS) metastases.

Source: NCI Thesaurus

Diseases studied

For each disease: the drug’s most advanced phase and active trials, with the reference trial on ClinicalTrials.gov.

DiseaseMost advanced phaseActive trialsReference trial
Chronic lymphocytic leukemiaIII3NCT07139873
Diffuse large B-cell lymphomaII–III2NCT07712588
Autoimmune thrombocytopenic purpuraII1NCT07294365

Everything on Birelentinib

In Phuturdex you get every trial with sponsors, countries and dates, development events, FDA and EMA approvals, patents and exclusivities, orphan designations and safety alerts, with PDF and Excel export. Free until 31 March 2027.

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Source: Phuturdex analysis of ClinicalTrials.gov (U.S. National Library of Medicine), FDA and EMA data, updated 13 November 2026. Active trials = recruiting or ongoing, phases I–III. Diseases are those named by each trial (NLM MeSH terms). The estimated launch, when shown, refers to the United States and is a Phuturdex calculation described on the Method page, not official data: the drug may already be marketed in other countries.

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