Cue Biopharma gets FDA fast track status for CUE-101 in HPV16+ R/M HNSCC

Pallavi Madhiraju- October 5, 2022 0

Cue Biopharma has been granted fast track designation for CUE-101 from the US Food and Drug Administration (FDA) for the treatment of a type of ... Read More

PDS Biotechnology gets FDA fast track status for PDS0101

pallavi123- June 5, 2022 0

PDS Biotechnology has secured fast track designation to its PDS0101 in combination with Merck’s KEYTRUDA (pembrolizumab) from the US Food and Drug Administration (FDA) for ... Read More

Seattle Genetics signs $4.4bn worth oncology deals with Merck

pharmanewsdaily- September 14, 2020 0

US biotech company Seattle Genetics has secured deals worth up to $4.4 billion with Merck, that include two new strategic oncology collaborations. The two major ... Read More

PADCEV, KEYTRUDA combination for advanced bladder cancer gets FDA breakthrough therapy status

pharmanewsdaily- February 20, 2020 0

PADCEV, KEYTRUDA combination : Astellas Pharma and Seattle Genetics said that the combination of PADCEV (enfortumab vedotin-ejfv) and Merck's anti-PD-1 therapy KEYTRUDA (pembrolizumab) has been ... Read More

Lilly launches LIBRETTO-431 clinical trial for selpercatinib in NSCLC

pharmanewsdaily- December 12, 2019 0

Eli Lilly and Company (Lilly) has initiated the phase 3 LIBRETTO-431 clinical trial to evaluate selpercatinib (LOXO-292) in RET fusion-positive non-small cell lung cancer (NSCLC) ... Read More

Merck secures EC approval for Keytruda in combination therapy for lung cancer

pharmanewsdaily- September 12, 2018 0

Merck has achieved a significant milestone by obtaining approval from the European Commission (EC) for its cancer immunotherapy, Keytruda (pembrolizumab), to be used in combination ... Read More

Alkermes expands Phase 1 trial of ALKS 4230 in combination with KEYTRUDA for advanced solid tumors

pharmanewsdaily- September 11, 2018 0

Irish biopharmaceutical company Alkermes has announced an expansion of its ongoing Phase 1 trial to evaluate the safety and anti-tumor activity of its immuno-oncology drug ... Read More

FDA approves Merck’s Keytruda in combination with chemotherapy for advanced lung cancer treatment

pharmanewsdaily- May 14, 2017 0

The US Food and Drug Administration (FDA) has granted approval to Merck’s cancer immunotherapy, Keytruda (pembrolizumab), in combination with chemotherapy, as a first-line treatment option ... Read More

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