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

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

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 with Eli Lilly’s chemotherapy drug pemetrexed (ALIMTA) and platinum chemotherapy. This approval specifically targets the first-line treatment of metastatic nonsquamous non-small cell lung cancer (NSCLC) in adults who do not […]

EC approves Novartis’ skin cancer therapy combo Tafinlar and Mekinist for melanoma

EC approves Novartis’ skin cancer therapy combo Tafinlar and Mekinist for melanoma

In a significant development for melanoma treatment, the European Commission (EC) has granted Novartis approval for its combination therapy of Tafinlar (dabrafenib) and Mekinist (trametinib). This approval is specifically for adjuvant therapy in stage III melanoma patients who are positive for the BRAF V600 mutation and have undergone complete surgical resection. The approval is based […]

Janssen secures EC approval for daratumumab as new multiple myeloma therapy

Janssen secures EC approval for daratumumab as new multiple myeloma therapy

The Janssen Pharmaceutical Companies of Johnson & Johnson have achieved a significant milestone with the European Commission’s approval of Darzalex (daratumumab) for use as an initial therapy in adult patients with newly diagnosed multiple myeloma who are not eligible for autologous stem cell transplant (ASCT). This approval allows for the combination of daratumumab with bortezomib, […]

EC grants expanded approval for Amgen’s BLINCYTO in pediatric acute lymphoblastic leukemia treatment

EC grants expanded approval for Amgen’s BLINCYTO in pediatric acute lymphoblastic leukemia treatment

In a significant development for pediatric oncology, the European Commission (EC) has approved an expanded indication for Amgen’s BLINCYTO (blinatumomab) as a monotherapy treatment for certain types of acute lymphoblastic leukemia (ALL) in children aged one year and older. This approval marks a crucial advancement in the treatment options available for this challenging medical condition. […]

EC approves Actelion’s Ledaga for treatment of cutaneous T-cell lymphoma

As per the Actelion recent news, the pharma’s Ledaga Chlormethine Gel 160 micrograms/g has been approved by the European Commission (EC) for CTCL MF treatment.

EC approves Actelion’s Ledaga for treatment of cutaneous T-cell lymphoma

The European Commission (EC) has granted marketing authorization to Actelion Pharmaceuticals for its innovative Ledaga Chlormethine Gel 160 micrograms/g, designed for the treatment of cutaneous T-cell lymphoma of the mycosis fungoides-type (CTCL MF). This approval marks a significant advancement in the treatment options available for this rare and often life-threatening immune system cancer. Breakthrough in […]