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BioWorld - Wednesday, May 6, 2026
Home » Authors » Tamra Sami

Articles by Tamra Sami

Acute myeloid leukemia illustration

GSK, LTZ partner to develop myeloid cell engagers

Nov. 19, 2025
By Tamra Sami
No Comments
Immunotherapy-focused biotech company LTZ Therapetics Inc. and GSK plc are partnering to develop up to four potential first-in-class myeloid cell engagers using LTZ’s immune-engager platform to target blood cancers and solid tumors.
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Jingsong Wang, CEO, Harbour Biomed
Cancer

Harbour Biomed launches AI-based antibody development platform

Nov. 19, 2025
By Tamra Sami
No Comments
Harbour Biomed is stepping up its antibody discovery process by using AI to develop innovative therapeutics. “We have done great through the traditional way of generating leads and designing molecules, but there’s a major gap as some therapeutics cannot reach the desired location or common targets,” Harbour Biomed founder, chairman and CEO Jingsong Wang told BioWorld.
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Komzifti packaging

FDA clears Kura/Kyowa’s Komzifti in r/r NPM1 mutant AML

Nov. 18, 2025
By Tamra Sami
The U.S. FDA gave the thumbs up to Kura Oncology Inc./Kyowa Kirin Co. Ltd.’s selective oral menin inhibitor, ziftomenib, to treat relapsed, refractory (r/r) nucleophosmin1 (NMP1)-mutant acute myeloid leukemia (AML). The approval of the drug, branded Komzifti, came more than two weeks ahead of the Nov. 30 PDUFA date.
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Nobel-prize-winner-Shimon-Sakaguchi-and-Adagene-CEO-Peter-Luo-11-14.jpg

Third Arc Bio licenses Adagene tech for CD3 T-cell engagers

Nov. 18, 2025
By Tamra Sami
No Comments
In a deal worth up to $840 million, Third Arc Bio Inc. is licensing Adagene Inc.’s Safebody technology platform to generate two masked CD3 T-cell engagers against unique tumor associated antigens.
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Doctor-patient consultation

J&J pushes to elevate patient voices in Asia

Nov. 18, 2025
By Tamra Sami
No Comments
Up to 77% of patients with non-small-cell lung cancer in Asia-Pacific rely almost entirely on their physicians to decide their treatment, even though 69% of physicians say they encourage shared decision-making. That disconnect remains one of the region’s biggest obstacles to improving outcomes, Anthony Elgamal, vice president of Oncology Asia Pacific at Johnson & Johnson Innovative Medicine, told BioWorld.
Read More
Jingsong Wang, CEO, Harbour Biomed

Harbour Biomed launches AI-based antibody development platform

Nov. 18, 2025
By Tamra Sami
No Comments
Harbour Biomed is stepping up its antibody discovery process by using AI to develop innovative therapeutics. “We have done great through the traditional way of generating leads and designing molecules, but there’s a major gap as some therapeutics cannot reach the desired location or common targets,” Harbour Biomed founder, chairman and CEO Jingsong Wang told BioWorld.
Read More
Haisheng Zhang, CEO, Signet
Cancer

Signet builds new model for gastric cancer drug discovery

Nov. 18, 2025
By Tamra Sami
No Comments
Signet Therapeutics founder Haisheng Zhang is betting on organoids and AI to outsmart diffuse gastric cancer and the limits of traditional “clean” drug design.
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Nobel-prize-winner-Shimon-Sakaguchi-and-Adagene-CEO-Peter-Luo-11-14.jpg

Third Arc Bio licenses Adagene tech for CD3 T-cell engagers

Nov. 14, 2025
By Tamra Sami
No Comments
In a deal worth up to $840 million, Third Arc Bio Inc. is licensing Adagene Inc.’s Safebody technology platform to generate two masked CD3 T-cell engagers against unique tumor associated antigens.
Read More
Cornerstone Robotics Sentire Surgical System

China’s Cornerstone Robotics raises $200M series D round

Nov. 14, 2025
By Tamra Sami
Cornerstone Robotics Ltd. raised an oversubscribed $200 million series D round to accelerate commercialization of its flagship product, the Sentire Endoscopic Surgical System.
Read More
Komzifti packaging

FDA clears Kura/Kyowa’s Komzifti in r/r NPM1 mutant AML

Nov. 13, 2025
By Tamra Sami
The U.S. FDA gave the thumbs up to Kura Oncology Inc./Kyowa Kirin Co. Ltd.’s selective oral menin inhibitor, ziftomenib, to treat relapsed, refractory (r/r) nucleophosmin1 (NMP1)-mutant acute myeloid leukemia (AML). The approval of the drug, branded Komzifti, came more than two weeks ahead of the Nov. 30 PDUFA date.
Read More
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