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Drugs in development · updated 13 November 2026

NBQ72S: clinical trials and development status

Other names and codes: QBS10072S

Development codeNot approved in the USNo EMA authorisation

As of 13 November 2026 NBQ72S is in 3 active clinical trials (recruiting or ongoing, phases I–III) for 5 diseases. The most advanced phase is 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 NBQ72S trials are recruiting

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3Active trials
IIMost advanced phase
5Diseases studied

What it is

A blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic chemotherapeutic domain, tertiary N-bis(2-chloroethyl)amine, linked to the structural features of a selective large amino acid transporter 1 (LAT1) substrate, with potential antineoplastic activity. Upon administration of QBS10072S, the LAT1 substrate binds to LAT1 expressed on the BBB and in LAT1-expressing cancer cells, such as glioblastoma multiforme (GBM). After entering the brain and binding to LAT1-expressing tumor cells, the cytotoxic domain in turn binds to DNA, causing cell cycle arrest and induces apoptosis. LAT1 is expressed at much lower levels in normal brain tissue and QBS10072S may therefore potentially target brain tumors while avoiding uptake by healthy, normal tissue.

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
Breast neoplasmII2NCT05305365
Brain NeoplasmsII1NCT05305365
GlioblastomaII1NCT02977780
Lung neoplasmII1NCT05305365
Meningeal neoplasmII1NCT05305365

Everything on NBQ72S

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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