Servier Egypt launches Tibsovo as first targeted therapy for IDH1-mutated cancers

Servier Egypt has launched Tibsovo (ivosidenib), the first targeted therapy available in the country for patients with IDH1-mutated Acute Myeloid Leukemia (AML) and intrahepatic cholangiocarcinoma. The treatment offers a median overall survival of 29.3 months for eligible AML patients and 10.3 months for those with intrahepatic cholangiocarcinoma, according to clinical data. It is approved as a first-line treatment for AML and a second-line option for intrahepatic cholangiocarcinoma.

Servier Egypt has introduced Tibsovo, a drug that targets the IDH1 genetic mutation in tumors, providing an alternative for patients with Acute Myeloid Leukemia (AML), an aggressive blood cancer originating in the bone marrow, and intrahepatic cholangiocarcinoma, a type of bile duct cancer starting inside the liver. This launch marks a significant step in expanding access to treatments addressing unmet medical needs in Egypt, where options have historically been limited for those unable to endure intensive chemotherapy or stem-cell transplantation.

Samy Sinnuqrut, General Manager of Servier Egypt, stated: “Bringing Tibsovo to Egypt is yet another step in Servier’s role to expand access to treatments that address clear medical needs. Our role is to ensure that these advances reach patients in a reliable and timely way.”

The AGILE clinical study showed improved event-free and overall survival for AML patients ineligible for intensive chemotherapy. The ClarIDHy study demonstrated better survival and disease control for intrahepatic cholangiocarcinoma patients. Ibtisam Saad El Din, Professor of Oncology at Cairo University, said: “The availability of Tibsovo gives physicians an important new tool for managing cancers driven by the IDH1 mutation. Identifying the mutation early through routine testing makes a significant difference in choosing the right treatment path.”

Tamer El Nahas, Oncology Consultant and Professor at Cairo University, added: “AML and cholangiocarcinoma often affect patients who cannot tolerate aggressive chemotherapy. Tibsovo provides a scientifically precise option with a more favourable tolerability profile.” Gamal Fathy, Professor of Haematology and Bone Marrow Transplant at the Nasser Institute, noted that the oral therapy delivers sustained clinical responses for AML patients and can reduce reliance on repeated transfusions.

Nearly 70% of Servier’s global research and development investment is focused on oncology. The therapy is recommended by international guidelines, including NCCN and ESMO.

Relaterade artiklar

Illustration of a Stanford researcher with briquilimab antibody vial in a lab, representing a new stem cell transplant method for Fanconi anemia.
Bild genererad av AI

Stanford-antikroppsregim möjliggör stamcells transplantationer utan strålning eller busulfan vid Fanconi-anemi

Rapporterad av AI Bild genererad av AI Faktagranskad

Ett Stanford Medicine-team rapporterar att en enda dos av anti-CD117-antikroppen briquilimab tillät tre barn med Fanconi-anemi att genomgå stamcells transplantationer utan strålning eller busulfan, och uppnådde nästan fullständig donorcellsintegration i en fas 1b-studie publicerad i Nature Medicine.

A Delhi High Court verdict on January 12 has allowed Indian pharma company Zydus Lifesciences to manufacture and sell a biosimilar version of Bristol Myers-Squibb's cancer drug Nivolumab. This ruling could pave the way for more affordable immunotherapy treatments for cancer patients in India. Nivolumab is effective against various cancers, with its patent set to expire in May 2026.

Rapporterad av AI

The US Food and Drug Administration (FDA) has approved mitapivat (brand name Aqvesme) for treating anaemia in adults with thalassaemia, working by improving red blood cell energy. The twice-daily pill can be taken by patients who need regular blood transfusions or those who do not. Experts say it could transform disease management in high-burden countries like India.

Brazil's National Health Surveillance Agency (Anvisa) approved the drug lecanemabe, marketed as Leqembi, on Thursday, January 8, for patients with early-stage Alzheimer's. The monoclonal antibody, administered via infusion, slows disease progression in individuals with mild cognitive impairment and confirmed beta-amyloid protein in the brain. The approval marks progress, though it is not a cure.

Rapporterad av AI Faktagranskad

Ett via kateter levererat implantat som långsamt frisätter gemcitabin eliminerade synliga tumörer hos 82% av patienter med BCG-oreagerande, hög-risk icke-muskelinvasiv blåscancer i en fas 2-studie. Mer än hälften av de som svarade förblev cancerfria i minst ett år, och enheten har sedan dess godkänts av FDA som Inlexzo för patienter med karcinom in situ som inte är kvalificerade för, eller avstår från, blåsans borttagning.

Brazil's Fiocruz, through its Farmanguinhos unit, has begun fully domestic production of tacrolimus, an immunosuppressant to prevent organ transplant rejection. The milestone stems from a Product Development Partnership (PDP) with Brazilian firm Libbs, which acquired manufacturing technology from India's Biocon. Farmanguinhos now becomes the sole supplier to the SUS public health system.

Rapporterad av AI

Ett omprofilerat bröstcancerläkemedel vid namn MDL-001 har visat lovande resultat i laboratorie- och djurstudier mot en rad virus, inklusive influensa, covid-19, RS-virus och norovirus. Läkemedlet, som utvecklats av det Kalifornienbaserade företaget Model Medicines med hjälp av AI, angriper en konserverad enzymdomän hos virus. En klinisk studie planeras till början av nästa år.

 

 

 

Denna webbplats använder cookies

Vi använder cookies för analys för att förbättra vår webbplats. Läs vår integritetspolicy för mer information.
Avböj