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Home » Authors » Tamra Sami

Articles by Tamra Sami

LTZ raises $20M to bring LTZ-301 to clinic for B-cell tumors

Aug. 6, 2024
By Tamra Sami
Immunotherapy-focused biotech company LTZ Therapetics Inc. raised $20 million in a series A round that will advance development of its myeloid engager pipeline to treat cancer and autoimmune diseases. Proceeds from the funds will accelerate development of lead asset LTZ-301, which is expected to enter the clinic in early 2025, LTZ founder and CEO Robert Li told BioWorld.
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Chinese flag and pills

China to deepen health care reforms, boost primary care capacity

Aug. 6, 2024
By Tamra Sami
China will deepen its health care reforms and will focus on enhancing its public health care capacity at the primary care level and at public hospitals, according to resolutions passed at the third plenary session of the 20th Central Committee of the Communist Party of China in July.
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Synchron Inc Stentrode brain implant

Synchron links brain implant device to Apple Vision Pro

Aug. 2, 2024
By Tamra Sami
Neurotech startup Synchron Inc. connected its brain implant to Apple’s Vision Pro headset, enabling patients with limited physical mobility to control the device using only their thoughts. Synchron is building an endovascular brain-computer interface designed to help patients with paralysis operate technology like smartphones and computers with their minds.
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LTZ raises $20M to bring LTZ-301 to clinic for B-cell tumors

Aug. 1, 2024
By Tamra Sami
Immunotherapy-focused biotech company LTZ Therapetics Inc. raised $20 million in a series A round that will advance development of its myeloid engager pipeline to treat cancer and autoimmune diseases. Proceeds from the funds will accelerate development of lead asset LTZ-301, which is expected to enter the clinic in early 2025, LTZ founder and CEO Robert Li told BioWorld.
Read More
Laptop displaying FDA logo

FDA issues refusal to file letter for Telix imaging agent

Aug. 1, 2024
By Tamra Sami
Radiopharmaceutical company Telix Pharmaceuticals Ltd. received a U.S. FDA refusal to file letter for its BLA seeking approval of renal cancer imaging agent TLX250-CDx (89Zr-DFO-girentuximab) for clear cell renal cell carcinoma (ccRCC).
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The Nasdaq Stock Exchange headquarters in New York

Radiopharm Theranostics to list on Nasdaq by year-end

July 31, 2024
By Tamra Sami

Radiopharm Theranostics Ltd. said it plans to list on Nasdaq by the end of 2024. The company had earlier announced plans to list in February 2023, but it delayed the listing due to market conditions.


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3D illustration showing presence of tumor inside prostate gland

Telix launches AU$650M bond offer, FDA accepts imaging NDA

July 30, 2024
By Tamra Sami
The U.S. FDA accepted Telix Pharmaceuticals Ltd.’s new drug application for TLX-007-CDx, a new cold kit for preparing prostate-specific membrane antigen-PET imaging for prostate cancer.
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EU flags in front of the Berlaymont building

A CHMP thumbs up for Astellas’ Claudin18.2 zolbetuximab

July 30, 2024
By Tamra Sami
Astellas Pharma Inc.’s claudin (CLDN) 18.2-targeted monoclonal antibody, zolbetuximab, received a positive opinion from the EMA’s Committee for Medicinal Products for Human Use (CHMP) and could be the first CLDN18.2 molecule to be approved in Europe if it receives final approval.
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Antibodies (light blue) and G protein-coupled receptors (purple)
Newco news

Alkira Bio exits stealth via seed round to develop GPCR-targeting antibodies

July 30, 2024
By Tamra Sami
Alkira Bio, a new spinout from Australia’s Florey Institute of Neuroscience and Mental Health has emerged from stealth mode thanks to seed funding from Curie.bio. Although the amount of funding is not disclosed, Curie.bio typically invests $5 million to $10 million in a founder company and then co-pilots the drug discovery program, deploying drug development experts to its portfolio companies to help navigate decision making as part of the deal, Florey researcher turned Alkira Bio CEO Daniel Scott told BioWorld.
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Monoclonal antibody illustration

European Commission approves Cstone PD-L1 sugemalimab in NSCLC

July 30, 2024
By Tamra Sami
The European Commission has approved Cstone Pharmaceuticals Ltd.’s PD-L1 monoclonal antibody, sugemalimab, in combination with platinum-based chemotherapy for first-line treatment of adults with metastatic non-small-cell lung cancer with no sensitizing EGFR mutations, or ALK, ROS1 or RET genomic tumor aberrations.
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