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Cancer treatments

NiKang Therapeutics
Regional

NiKang Advances CDK2 Degrader with Key Milestone in Cancer Treatment Trial

March 16, 2025March 15, 2025 - by Timothy Alexander

WILMINGTON, DE — NiKang Therapeutics® Inc. has achieved a pivotal step in the development of its first-in-class CDK2 degrader, NKT3964, by completing the dosing of the first patient cohort in a …

NiKang Advances CDK2 Degrader with Key Milestone in Cancer Treatment Trial Read More

Third Arc Bio
Regional

Third Arc Bio Enters Clinical Stage with First Patient Dosed in ARC101 Study

March 16, 2025March 15, 2025 - by Timothy Alexander

SPRING HOUSE, PA — Third Arc Bio Inc. has administered the first dose of ARC101 to a patient in its inaugural first-in-human clinical trial. This milestone marks the company’s transition to …

Third Arc Bio Enters Clinical Stage with First Patient Dosed in ARC101 Study Read More
The Wistar Institute
Cancer / Regional

Wistar Institute Uncovers New Strategy for Treating Resistant Melanoma

February 7, 2025February 6, 2025 - by Timothy Alexander

PHILADELPHIA, PA— Researchers at The Wistar Institute, led by Jessie Villanueva, Ph.D., have made significant strides in combating treatment-resistant melanoma. Their latest discovery focuses on inhibiting the gene S6K2, a breakthrough …

Wistar Institute Uncovers New Strategy for Treating Resistant Melanoma Read More

Context Therapeutics
Regional

BioAtla and Context Therapeutics Forge Strategic Agreement for Cancer Treatment Development

September 25, 2024September 25, 2024 - by Timothy Alexander

SAN DIEGO, CA and PHILADELPHIA, PA — BioAtla, Inc. and Context Therapeutics Inc. have entered into a significant agreement, granting Context an exclusive, worldwide license to develop and commercialize BioAtla’s BA3362, …

BioAtla and Context Therapeutics Forge Strategic Agreement for Cancer Treatment Development Read More
Prelude Therapeutics
Regional

Prelude Therapeutics Releases Promising Phase 1 Data on Novel Cancer Treatment

September 14, 2024September 13, 2024 - by Timothy Alexander

WILMINGTON, DE — Prelude Therapeutics Incorporated this week unveiled interim results from its Phase 1 trial of PRT3789, a pioneering therapy designed to target cancers with a SMARCA4 mutation. The data, …

Prelude Therapeutics Releases Promising Phase 1 Data on Novel Cancer Treatment Read More

Panavance Therapeutics
Cancer / Research

Panavance Therapeutics Reports Positive Data on Misetionamide in Ovarian Cancer

August 15, 2024August 14, 2024 - by Timothy Alexander

BERWYN, PA — Panavance Therapeutics Inc. has announced the publication of encouraging data on misetionamide in the peer-reviewed journal, Cancer Medicine. The study conducted by Kim et al. at MD …

Panavance Therapeutics Reports Positive Data on Misetionamide in Ovarian Cancer Read More
Context Therapeutics
Regional

Context Therapeutics Acquires Promising Cancer Treatment Asset

July 10, 2024July 10, 2024 - by Timothy Alexander

PHILADELPHIA, PA — Context Therapeutics Inc. (Nasdaq: CNTX) announced a significant addition to its drug pipeline with the acquisition of CT-95 from Link Immunotherapeutics, Inc. The asset is a mesothelin …

Context Therapeutics Acquires Promising Cancer Treatment Asset Read More

Prelude Therapeutics
Regional

Prelude Therapeutics Joins Forces with Merck for Cancer Treatment Trial

July 9, 2024July 9, 2024 - by Timothy Alexander

WILMINGTON, DE — Prelude Therapeutics Incorporated (Nasdaq: PRLD) has announced a collaboration with Merck to evaluate a new cancer treatment. The Phase 2 clinical trial will test Prelude’s investigational drug, …

Prelude Therapeutics Joins Forces with Merck for Cancer Treatment Trial Read More
Food and Drug Administration
Cancer / National

FDA Announces End to National Shortage of Crucial Cancer Drug Cisplatin

July 5, 2024July 2, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The Food and Drug Administration (FDA) has announced that the national supply of cisplatin, a key cancer medication, now exceeds demand, ending a critical shortage that began …

FDA Announces End to National Shortage of Crucial Cancer Drug Cisplatin Read More
Food and Drug Administration
Cancer / National

FDA Grants Accelerated Approval to New Treatment for Relapsed Follicular Lymphoma

July 5, 2024July 2, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The Food and Drug Administration (FDA) recently granted accelerated approval to Epkinly (epcoritamab-bysp), a new treatment option for adults with relapsed or refractory follicular lymphoma (FL). This …

FDA Grants Accelerated Approval to New Treatment for Relapsed Follicular Lymphoma Read More

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