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Drugs in development · updated 11 November 2026

Avotaciclib: clinical trials and development status

Other names and codes: BEY1107

FDA substance registryNot approved in the USNo EMA authorisation

As of 11 November 2026 Avotaciclib is in 3 active clinical trials (recruiting or ongoing, phases I–III) for 3 diseases. The most advanced phase is I–II.

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 Avotaciclib trials are recruiting

Map of sites in Europe with recruitment status, every trial and an email when something changes. Full access free until 31 March 2027, no card needed.

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3Active trials
I–IIMost advanced phase
3Diseases studied

What it is

An orally bioavailable, cyclin dependent kinase 1 (CDK1) inhibitor, with potential antineoplastic activity. Upon administration, avotaciclib targets, binds to and inhibits the activity of CDK1. This may inhibit cancer stem cell (CSC) division, cause cell cycle arrest, and induce apoptosis. This may inhibit tumor cell proliferation. CDK1, an ATP-dependent serine/threonine kinase, plays a key role in regulating cell division, cell cycle progression and proliferation. It is frequently overexpressed in tumor cells.

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
Colorectal neoplasmI–II1NCT05093907
Pancreatic neoplasmI–II1NCT03579836
GlioblastomaI1NCT05769660

Everything on Avotaciclib

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 11 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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