IPP Bureau

Lupin appoints Abdelaziz Toumi as CEO of its API CDMO subsidiary
Lupin appoints Abdelaziz Toumi as CEO of its API CDMO subsidiary

By IPP Bureau - June 17, 2024

Abdel has held leadership positions at Bayer, Merck, Catalent, Lonza, and KBI Biopharma,

Health Minister J P Nadda takes review meeting of Department of Pharmaceuticals
Health Minister J P Nadda takes review meeting of Department of Pharmaceuticals

By IPP Bureau - June 17, 2024

Department presents a detailed overview of the Pharma and MediTechsector and gives a detailed presentation on the activities of Department

Imfinzi approved in the US for endometrial cancer
Imfinzi approved in the US for endometrial cancer

By IPP Bureau - June 17, 2024

Approval based on DUO-E trial results, which showed Imfinzi reduced the risk of disease progression or death by 58% vs. chemotherapy

Lupin and Fuji sign agreement for commercialization of Nextstellis in Vietnam and Philippines
Lupin and Fuji sign agreement for commercialization of Nextstellis in Vietnam and Philippines

By IPP Bureau - June 17, 2024

Alembic announces USFDA final approval for Icatibant injection
Alembic announces USFDA final approval for Icatibant injection

By IPP Bureau - June 17, 2024

This is the first peptide product approval from the USFDA received by Alembic Pharmaceuticals

Calquence plus chemoimmunotherapy reduced the risk of disease progression or death by 27%
Calquence plus chemoimmunotherapy reduced the risk of disease progression or death by 27%

By IPP Bureau - June 17, 2024

First and only BTK inhibitor to demonstrate favourable overall survival trend vs. standard-of-care chemoimmunotherapy in this setting

USFDA approves next-gen TKI Augtyro for treatment of solid tumors
USFDA approves next-gen TKI Augtyro for treatment of solid tumors

By IPP Bureau - June 17, 2024

Augtyro is the only FDA-approved treatment option for NTRK-positive tumors studied in both TKI-naïve and TKI-pretreated patients across solid tumors

Health Minister Nadda aims to attain targeted Health goals in the first 100 days of formation of new government
Health Minister Nadda aims to attain targeted Health goals in the first 100 days of formation of new government

By IPP Bureau - June 15, 2024

Nadda expressed his concern about growing incidence of Non-Communicable Diseases and the importance of awareness regarding healthy diet and lifestyle

Fischer Medical Ventures and The Therapy Platform partner for mental healthcare
Fischer Medical Ventures and The Therapy Platform partner for mental healthcare

By IPP Bureau - June 15, 2024

Fischer MVL envisages to offer a diverse portfolio of diagnostic solutions

Jubilant Draximage to invest US$ 50 million to expand its PET radiopharmacy network
Jubilant Draximage to invest US$ 50 million to expand its PET radiopharmacy network

By IPP Bureau - June 15, 2024

Jubilant's Radiopharma Business to expand positron emission tomography radiopharmacy network

Sun Pharma and Moebius Medical present Phase 2b study on MM-II
Sun Pharma and Moebius Medical present Phase 2b study on MM-II

By IPP Bureau - June 15, 2024

There is an urgent need for more therapeutic treatment options for patients with painful osteoarthritis

Jubilant Pharmova announces voluntary prepayment of US$ 75 million term loan
Jubilant Pharmova announces voluntary prepayment of US$ 75 million term loan

By IPP Bureau - June 15, 2024

As on 31st March 2024, Jubilant Pharmova Limited reported Gross Debt at Rs. 3,414 crore

Moderna announces positive Phase 3 efficacy data for next generation COVID-19 vaccine
Moderna announces positive Phase 3 efficacy data for next generation COVID-19 vaccine

By IPP Bureau - June 14, 2024

Higher efficacy was observed in mRNA-1283 compared to Spikevax in adults 18 years of age and older

USFDA approves expanded age indication for GSK’s RSV vaccine ‘Arexvy’
USFDA approves expanded age indication for GSK’s RSV vaccine ‘Arexvy’

By IPP Bureau - June 14, 2024

Over 13 million US adults aged 50-59 years have a medical condition that increases their risk of severe RSV outcomes

Farxiga approved in the US for the treatment of paediatric type-2 diabetes
Farxiga approved in the US for the treatment of paediatric type-2 diabetes

By IPP Bureau - June 14, 2024

Approval based on results from T2NOW, one of the largest paediatric type-2 diabetes Phase III trials to date

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