IPP Bureau

Mandaviya visits Jan Aushadhi stall at IITF
Mandaviya visits Jan Aushadhi stall at IITF

By IPP Bureau - November 21, 2023

Jan Ausahdhi exhibited demonstration stall during 42nd India International Trade Fair to spread awareness

Mandaviya visits Ayushman Bhav Health Pavilion at the 42nd IITF 2023
Mandaviya visits Ayushman Bhav Health Pavilion at the 42nd IITF 2023

By IPP Bureau - November 21, 2023

Distributes Ayushman cards to several beneficiaries

AstraZeneca launches health-tech business ‘Evinova’
AstraZeneca launches health-tech business ‘Evinova’

By IPP Bureau - November 21, 2023

Evinova will operate as a separate health-tech business within AstraZeneca

GSK receives positive CHMP opinion recommending momelotinib for myelofibrosis patients with anaemia
GSK receives positive CHMP opinion recommending momelotinib for myelofibrosis patients with anaemia

By IPP Bureau - November 21, 2023

Decision on EU marketing authorisation expected for momelotinib by early 2024

Oceanic-AF study stopped early due to lack of efficacy
Oceanic-AF study stopped early due to lack of efficacy

By IPP Bureau - November 21, 2023

OCEANIC-AF is one trial which evaluates asundexian versus apixaban in patients with atrial fibrillation at risk for stroke within the overall OCEANIC phase III program

Strides receives USFDA approval for Levetiracetam Oral Solution
Strides receives USFDA approval for Levetiracetam Oral Solution

By IPP Bureau - November 21, 2023

The product is bioequivalent and therapeutically equivalent to the Reference Listed Drug (RLD) and is used in the treatment of seizures.

Health Minister Mandaviya delivers keynote address 2nd Voice of Global South Summit 2023
Health Minister Mandaviya delivers keynote address 2nd Voice of Global South Summit 2023

By IPP Bureau - November 20, 2023

Emphasizes the need for a collective effort on bolstering resilience across economies, societies, healthcare systems, education systems and infrastructure

AskBio announces first patient randomized in Phase 1 Trial of AB-1005
AskBio announces first patient randomized in Phase 1 Trial of AB-1005

By IPP Bureau - November 20, 2023

Gene therapy AB-1005 being developed to locally increase glial cell line-derived neurotrophic factor (GDNF) levels

Lupin receives approval from US FDA for Ganirelix Acetate Injection
Lupin receives approval from US FDA for Ganirelix Acetate Injection

By IPP Bureau - November 20, 2023

The product will be manufactured at Lupin’s Nagpur facility in India

Teva announces approval of a generic version of Forteo in US
Teva announces approval of a generic version of Forteo in US

By IPP Bureau - November 20, 2023

This approval showcases Teva’s proven strengths in complex generic formulations development and device engineering

Dr. Reddy's rolls out drug-free non-invasive migraine management device ‘Nerivio’ in India
Dr. Reddy's rolls out drug-free non-invasive migraine management device ‘Nerivio’ in India

By IPP Bureau - November 17, 2023

Nerivio is a prescription-based non-invasive device intended for acute and prophylactic (preventive) treatment of migrain

Alkem healthy lungs initiative to promote importance of inhalation therapy
Alkem healthy lungs initiative to promote importance of inhalation therapy

By IPP Bureau - November 17, 2023

The countrywide initiative aims to spread awareness, educate the public & ensure that no one is left behind in the fight against respiratory diseases

FDA approves Merck’s Keytruda plus chemotherapy as first line treatment for locally advanced Metastatic HER2-Negative Gastric
FDA approves Merck’s Keytruda plus chemotherapy as first line treatment for locally advanced Metastatic HER2-Negative Gastric

By IPP Bureau - November 17, 2023

Approval based on results from the Phase 3 KEYNOTE-859 trial, which demonstrated significant improvement in overall survival in these patients versus chemotherapy alone

Brenntag Specialties and Zeochem expand collaboration for Pharma EMEA
Brenntag Specialties and Zeochem expand collaboration for Pharma EMEA

By IPP Bureau - November 17, 2023

Collaboration enables Brenntag to serve pharma customers in EMEA with chromatography silica gels

Pfizer and Astellas' XTANDI approved by USFDA in earlier prostate cancer treatment setting
Pfizer and Astellas' XTANDI approved by USFDA in earlier prostate cancer treatment setting

By IPP Bureau - November 17, 2023

XTANDI becomes the first and only androgen receptor signaling inhibitor approved for use with or without a GnRH analog therapy in nonmetastatic castration-sensitive prostate cancer

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