Neok plays a high-risk bispecific conjugate game
Armed with $75m the company takes a risky asset into the clinic.
Armed with $75m the company takes a risky asset into the clinic.
Shortly after closing a $75m venture capital fund raising Neok Bio is set to become a clinical-stage biotech, on Wednesday receiving US clearance to begin a phase 1 trial of a bispecific ADC coded NEOK001. But it’s the antigens that this molecule hits – B7-H3 and ROR1 – that should give pause.
The former is the target of Daiichi Sankyo/Merck & Co’s ifinatamab deruxtecan, which has just spent time on clinical hold, while the latter has been associated with discontinuations at Oncternal Therapeutics and Lyell, and toxicity worries at Merck. Neok’s approach is not for the faint of heart.
That’s not to say that NEOK001 is destined to fail, of course, as each project has its own unique characteristics. But there’s little to suggest that NEOK001 is especially differentiated – it comprises a typical topoisomerase 1 inhibitor payload, for instance – and Neok could certainly have played it safer in choosing its first clinical asset.
South Korean offshoot
The company is formally based in California, but is essentially an offshoot of South Korea’s ABL Bio, and came out of stealth mode last November with the announced fund raising, a $75m series A.
ABL has interests in therapy areas outside oncology, while its cancer pipeline includes ragistomig, an anti-PD-L1 x 4-1BB naked MAb, as well as monospecific ADCs and givastomig, an anti-Claudin18.2 bispecific developed in collaboration with NovaBridge Biopharma. NovaBridge was until last October known as I-Mab, and its work with ABL dates back to 2018, covering several assets.
However, it's two bispecific ADCs that ABL has spun into Neok, and the private company’s declared focus is on such dual-acting conjugates. Neok’s other currently disclosed pipeline asset besides NEOK001 is NEOK002, an ADC against EGFR and Muc1 that the company expects to enter clinical trials this year, in tandem with NEOK001.
However, there is no news yet about an IND filing for NEOK002, though one is expected imminently. Attention now falls to the first clinical data from NEOK001’s phase 1 trial, something Neok hopes to be ready to unveil next year.
Selected oncology assets owned by ABL Bio
| Project | Mechanism | Source/ownership |
|---|---|---|
| Givastomig | Claudin18.2 x 4-1BB MAb | Jun 2018 collaboration between ABL and I-Mab (now known as NovaBridge) |
| Ragistomig | PD-L1 x 4-1BB MAb | Jun 2018 collaboration between ABL and I-Mab (now known as NovaBridge) |
| ABL202/ LCB71/ CS5001 | ROR1 ADC | Jul 2016 collaboration between ABL and LigaChem (now known as LegoChem), licensed to CStone in Nov 2020 |
| Tovecimig | DLL4 x VEGF-A MAb | Nov 2018 licence to Trigr Therapeutics (in May 2021 acquired by Compass Therapeutics) |
| ABL206/ NEOK001 | B7-H3 x ROR1 ADC | Spun into Neok Bio in Jul 2024 |
| ABL209/ NEOK002 | EGFR x Muc1 ADC | Spun into Neok Bio in Jul 2024 |
| ABL102/ TRIA0201 | ROR1 x 4-1BB MAb | Nov 2018 licence to Trigr Therapeutics (terminated in May 2021) |
| ABL103/ TRIA002 | B7-H4 x 4-1BB MAb | Nov 2018 licence to Trigr Therapeutics (terminated in May 2021) |
| ABL104/ YH32364 | EGFR x 4-1BB MAb | Sep 2018 collaboration between ABL and Yuhan |
| ABL105 | HER2 x 4-1BB MAb | Sep 2018 collaboration between ABL and Yuhan |
Source: OncologyPipeline.
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