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Drugs in development · updated 11 November 2026

Nezutatug: clinical trials and development status

Other names and codes: HMBD-001

FDA substance registryNot approved in the USNo EMA authorisation

As of 11 November 2026 Nezutatug is in 3 active clinical trials (recruiting or ongoing, phases I–III) for 15 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 Nezutatug 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
15Diseases studied

What it is

A humanized immunoglobulin G1 (IgG1) monoclonal antibody directed against the human epidermal growth factor receptor 3 (HER3; ERBB3), with potential antineoplastic activity. Upon administration, nezutatug targets and binds to HER3 and inhibits its activation. This may prevent HER3-mediated signaling and inhibit HER3-dependent tumor cell proliferation and differentiation. HER3, a member of the epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases, is frequently overexpressed in tumors and is associated with poor prognosis and drug resistance; it has no active kinase domain but is activated through heterodimerization with other members of the EGFR receptor family, such as HER2.

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
Non-small-cell lung carcinomaI–II3NCT05910827
Pancreatic neoplasmI–II2NCT05057013
Bladder neoplasmI–II1NCT05057013
Castration-resistant prostatic neoplasmI–II1NCT05057013
Endometrial neoplasmI–II1NCT05057013
Esophageal neoplasmI–II1NCT05057013
Head and neck squamous cell carcinomaI–II1NCT05910827
Hepatocellular carcinomaI–II1NCT05057013
MelanomaI–II1NCT05057013
Ovarian neoplasmI–II1NCT05057013
Squamous cell carcinomaI–II1NCT05910827
Stomach neoplasmI–II1NCT05057013
Triple-negative breast neoplasmI–II1NCT05057013
Uterine cervix neoplasmI–II1NCT05057013
MetastasisI1NCT05919537

Sites in Europe

4 sites of the active trials in one European country, 0 recruiting.

Sites declared by the sponsors on ClinicalTrials.gov; region worked out by Phuturdex from the geographic point. The list of sites with city and recruitment status is in the app. See the sites →

Everything on Nezutatug

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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