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BioWorld - Tuesday, April 14, 2026
Home » solid tumors

Articles Tagged with ''solid tumors''

3D illustration of tumor
Cancer

Nuvation’s NUV-1511 receives FDA clearance for phase I/II study in solid tumors

Jan. 9, 2024
Nuvation Bio Inc. has received FDA clearance of its IND application to evaluate NUV-1511 in a phase I/II study for solid tumors.
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Antibodies attacking cancer cell
Immuno-oncology

Immunome licenses Zentalis’ ROR1 ADC and platform technology

Jan. 9, 2024
Immunome Inc. and Zentalis Pharmaceuticals Inc. have entered into an exclusive, worldwide license agreement.
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Handshake, money, calculator, MA-letters

J&J kicks off JPM 2024 with $2B offer for ADC firm Ambrx

Jan. 8, 2024
By Jennifer Boggs
The zeal for antibody-drug conjugates (ADCs), a prominent focus for dealmaking in 2023, shows no signs of waning, as Johnson & Johnson greeted attendees of the J.P. Morgan Healthcare Conference (JPM) with news of its $2 billion buyout of Ambrx Biopharma Inc., picking up rights to an ADC platform along with a promising candidate targeting advanced prostate cancer. Under the terms, J&J agreed to acquire all outstanding shares of San Diego-based Ambrx for $28 apiece, marketing a 105% premium to the firm’s Jan. 5 closing price. Unsurprisingly, Ambrx’s stock (NASDAQ:AMAM) gained 101.5% to close Jan. 8 at $27.47.
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Cancer

Onkure's PI3Kα H1047R inhibitor OKI-219 cleared to enter clinic for solid tumors

Jan. 5, 2024
Onkure Inc. has received FDA clearance of its IND application for OKI-219, a mutant selective PI3Kα H1047R inhibitor, for solid tumors.
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Cancer

Quanta advances KRAS inhibitor pipeline with IND, candidate selection

Jan. 5, 2024
Quanta Therapeutics Inc. has announced progression of its pipeline of KRAS-directed drug candidates, with the receipt of IND approval from the FDA for QTX-3034.
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Allorion’s CDK2 inhibitor at center of potential $1B licensing deal with Avenzo

Jan. 4, 2024
Amid a flurry of dealmaking activity to start 2024, Allorion Therapeutics Inc., a 2020 startup based in Natick, Mass., and Guangzhou, China, has been extra busy. Two days after disclosing a potential $540 million deal with Astrazeneca plc, Allorion inked a licensing agreement with Avenzo Therapeutics Inc. that could total more than $1 billion.
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Antibody-drug conjugate

Medilink nets second $1B deal, out-licenses ADC to Roche

Jan. 3, 2024
By Marian (YoonJee) Chu
Three months out from its first $1 billion deal with Biontech SE for an antibody-drug conjugate (ADC), Suzhou, China-based Medilink Therapeutics Co. Ltd. clinched another potential $1 billion ADC deal, but this time with Roche Holding AG.
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Cancer

Pasithea’s macrocyclic MEK inhibitor cleared by FDA to enter clinic for advanced solid tumors

Jan. 3, 2024
Pasithea Therapeutics Corp. has received IND clearance by the FDA to evaluate PAS-004, a small-molecule allosteric inhibitor of MEK 1/2.
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Art concept for tumor
Immuno-oncology

Medilink collaborates with Roche to advance ADC for solid tumors

Jan. 3, 2024
Medilink Therapeutics (Suzhou) Co. Ltd. has entered into a worldwide collaboration and license agreement with F. Hoffmann-La Roche Ltd. for the development of YL-211, a next-generation antibody-drug conjugate candidate targeting proto-oncogene c-Met for solid tumors.
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Antibody-drug conjugate illustration
Immuno-oncology

Obi Pharma to advance TROP2-targeted ADC into clinic in US

Jan. 3, 2024
Obi Pharma Inc. has received FDA clearance for its IND application to conduct a phase I/II study of OBI-992, a novel antibody-drug conjugate (ADC) cancer therapy targeting TROP2. The trial will open shortly and aims to enroll patients with advanced solid tumors, including non-small-cell lung cancer, small-cell lung cancer and gastric cancer, although several other cancers are also potential targets.
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