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Boundless and others head for phase 1

First-in-human study initiations include Boundless Bio’s second asset, and an ADC from Tubulis.

Boundless Bio, the biotech hoping soon to go public, has taken its second pipeline asset into the clinic. Its lead focus is CHK1 inhibition, but the asset newly into phase 1 is the RNR inhibitor BBI-825 – a mechanism of action that appears to have no industry competition.

Its solid tumour study, which began last month, appears among the latest first-in-human initiations, according to recently unveiled clinicaltrials.gov listings. These also include a multiple myeloma Car-T project in development by a biotech more famous for autoimmune disease cell therapy, and an ADC from Tubulis, a German group that yesterday closed a €128m private financing.

Tubulis has two lead ADCs, but TUB-040, which targets NaPi2b, is the first that appears headed for the clinic. Its Napistar1-01 study, in ovarian and lung cancers, is due to begin in May – presumably once the proceeds of the €128m series B round, co-led by EQT Life Sciences and Nextech Invest, have been safely banked.

TUB-040 uses a cleavable linker, has a drug-to-MAb ratio of eight, and uses a topoisomerase 1 inhibitor payload, a currently popular strategy. Meanwhile, NaPi2b is a fairly rare target to go after, and Mersana’s discontinuation of upifitamab rilsodotin and XMT-1592 left Zymeworks and ADC Therapeutics among the few other active players.

Meanwhile, in RNR inhibition the only competitor to Boundless’s BBI-825 is an academic study run by the NCI/City of Hope, according to OncologyPipeline.

mRNA Car-T therapy

In cell therapy Cartesian Therapeutics has pursued the concept, recently gaining much traction, of targeting not cancer but autoimmune disease. However, its latest clinical effort will feature Descartes-15, an autologous anti-BCMA Car generated by mRNA and not requiring lymphodepletion, in multiple myeloma.

Also in vogue, judging by the number of recent deals struck, is radioligand therapy, and Radiopharm Theranostics’ RAD204 combines the radioactive isotope lutetium-177 with a camelid-derived nanobody that targets PD-L1. Radiopharm, a listed Australian company, gained this asset through the acquisition of NanoMab, and is developing it in collaboration with Lantheus.

The trial, being carried out in Australia, will enrol PD-L1-positive NSCLC patients; in 2022 Radiopharm said this would begin “shortly”, but it is only now getting under way. OncologyPipeline reveals no other radiotherapeutics targeting PD-(L)1 in clinical development.

Finally, the anti-CCR8 MAb HC006 is being taken into a phase 1 solid tumour study by HC Biopharma. This should be of interest to Coherus, which was developing an in-house CCR8 inhibitor before paying $65m in stock to acquire Surface Oncology, which brought with it the anti-CCR8 MAb SRF114.

Coherus’s idea is to combine SRF114 with its recently approved anti-PD-1 MAb Loqtorzi. However, the trial of HC006 tests monotherapy only.

 

Recently disclosed first-in-human studies*

ProjectMechanismCompanyTrialScheduled start
HC006Anti-CCR8 MAbHC BiopharmaSolid tumours27 Feb 2024
BBI-825RNR inhibitorBoundless BioSolid tumours29 Feb 2024
PAS-004MEK 1/2 inhibitorPasithea TherapeuticsSolid tumours29 Feb 2024
Descartes-15BCMA mRNA Car-TCartesian Therapeuticsr/r multiple myeloma1 Mar 2024
IPN01194ERK1/2 inhibitorIpsenSolid tumours14 Mar 2024
INI-4001TLR7/8 agonistInimmuneSolid tumours29 Mar 2024
RAD204/ NM-01Lutetium-177 labelled anti-PD-L1 nanobodyRadiopharm/ LantheusPD-L1+ve NSCLCMar 2024
SCTB14Anti-PD-1 x VEGF MAbSinocelltechSolid tumours30 Apr 2024
SRG-514UndisclosedSurge TherapeuticsAdjuvant breast cancerApr 2024
TUB-040Anti-NaPi2b ADCTubulisNapistar1-01, ovarian & adeno NSCLCMay 2024

Note: *projects newly listed on the clinicaltrials.gov database between 8 and 12 Mar 2024.