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Lenvima

Japan approves Keytruda plus Lenvima combination for endometrial cancer treatment

Keytruda Lenvima endometrial cancer

the Ministry of Health, Labour and Welfare (MHLW) of Japan has approved Keytruda plus Lenvima combination to treat endometrial carcinoma.

December 28, 2021 by drugs

European Commission Approves KEYTRUDA Plus LENVIMA for Patients With Endometrial Carcinoma

chemotherapy LENVIMA KEYTRUDA Endometrial Carcinoma

Merck and Eisai announced that the European Commission has approved the combination of KEYTRUDA, Merck’s anti-PD-1 therapy, plus LENVIMA, the orally available multiple receptor tyrosine kinase inhibitor discovered by Eisai, for the treatment of advance...

December 2, 2021 by AmericanPharmaceuticalReview

EC grants approval for Merck-Eisai’s combo therapy for endometrial cancer

Lenvima tyrosine kinase endometrial cancer

The European Commission (EC) has granted approval for Merck (MSD) and Eisai’s Keytruda (pembrolizumab) in combination with Lenvima (lenvatinib) to treat adults with advanced or recurrent endometrial cancer.

December 1, 2021 by Pharmaceutical-Technology

FDA approves Keytruda plus Lenvima for advanced kidney cancer

FDA Keytruda RCC Eisai Lenvima

The US Food and Drug Administration (FDA) has approved a combination of MSD’s anti-PD-1 therapy Keytruda (pembrolizumab) plus Eisai’s Lenvima (lenvatinib) for the first-line treatment of adult patients with advanced renal cell carcinoma ...

August 13, 2021 by pharmatimes

US clears Keytruda, Lenvima combo in first-line kidney cancer

Keytruda Lenvima kidney cancer

The FDA announced Wednesday that it approved the combination of Merck & Co.'s anti-PD-1 therapy Keytruda (pembrolizumab) and Eisai's oral multi-kinase inhibitor Lenvima (lenvatinib) as a first-line treatment for adults with advanced renal cell carcinoma.

August 12, 2021 by firstwordpharma

FDA Approves Keytruda (pembrolizumab) Plus Lenvima (lenvatinib) Combination for Patients With Certain Types of Advanced Endometrial Carcinoma

FDA Keytruda Lenvima

Merck (NYSE: MRK), known as MSD outside the United States and Canada, and Eisai Inc. today announced that the U.S. Food and Drug Administration (FDA) has approved the combination of Keytruda, Merck’s anti-PD-1 therapy, plus Lenvima.

July 29, 2021 by drugs

Eisai, Merck’s Drug Combo Approved for Advanced Endometrial Cancer

Eisai Merck LENVIMA dMMR KEYTRUDA

LENVIMA plus KEYTRUDA demonstrates improvements in overall survival, reducing the risk of death by 32%, and progression-free survival by 40%.

July 26, 2021 by contractpharma

Eisai’s anti-cancer agent LENVIMA receives orphan drug designation

Eisai LENVIMA uterine body cancer

Japanese pharmaceutical company Eisai has received orphan drug designation for its anti-cancer agent LENVIMA with a prospective indication for uterine body cancer.

March 16, 2021 by pharmaceutical-technology

Merck reports positive results for Keytruda, Lenvima combo in phase 3 KEYNOTE-775/Study 309 trial

Merck KEYNOTE-775 Keytruda Lenvima Study 309

Merck and Eisai announced that the pivotal Phase 3 KEYNOTE-775/Study 309 trial evaluating the investigational use of KEYTRUDA, Merck’s anti-PD-1 therapy, plus LENVIMA, the orally available multiple receptor tyrosine kinase inhibitor discovered by Eisai ..

December 21, 2020 by pharmaceutical-business-review

Lenvima plus Keytruda achieves primary endpoints in trial for RCC

Lenvima Keytruda Eisai RCC

Lenvima and Keytruda has demonstrated positive top-line results in a Phase III trial in patients with advanced renal cell carcinoma.

November 12, 2020 by europeanpharmaceuticalreview

Keytruda/Lenvima combo shows promise in hard-to-treat cancers

Keytruda Lenvima cancer Eisai Merck

MSD (Merck) and Eisai have revealed new data from two trials under the LEAP clinical programme evaluating the combination of MSD’s PD-1 inhibitor Keytruda and Eisai’s oral tyrosine kinase inhibitor Lenvima.

September 22, 2020 by pharmatimes

US rejects MSD/Eisai's Keytruda Lenvima combo

Keytruda Lenvima MSD Eisai

MSD and Eisai have received a complete response letter (CRL) from the US Food and Drug Administration rejecting accelerated approval of a combination of Keytruda (pembrolizumab) and Lenvima (lenvatinib) for liver cancer.

July 10, 2020 by pharmatimes