IPP Bureau

BASF Pharma Solutions excipient accepted into FDA Pilot Program
BASF Pharma Solutions excipient accepted into FDA Pilot Program

By IPP Bureau - December 06, 2022

Soluplus branded excipient play a critical role in enabling the drug development process for poorly soluble active pharmaceutical ingredients

JB Pharma reduces price of Azmarda by 50%
JB Pharma reduces price of Azmarda by 50%

By IPP Bureau - December 06, 2022

Move to increase affordability and accessibility for heart failure patients across the country

Indira IVF to offer fertility perks for Indian corporate employees
Indira IVF to offer fertility perks for Indian corporate employees

By IPP Bureau - December 06, 2022

The service includes full fertility care benefits, including egg and embryo freezing options to employees

ANSSI Wellness inaugurates its new spine clinic in Pune
ANSSI Wellness inaugurates its new spine clinic in Pune

By IPP Bureau - December 06, 2022

Asia’s premier and USA-patented, ANSSI Wellness for spinal decompression was launched in Pune

ASG Eye Hospitals opens hospital in Vashi
ASG Eye Hospitals opens hospital in Vashi

By IPP Bureau - December 06, 2022

The new eye hospital in Vashi is ASG’s second in the Mumbai Metropolitan Region (MMR) and the sixth in Maharashtra

Auretics launched herbal cough syrup ‘Sedoril’
Auretics launched herbal cough syrup ‘Sedoril’

By IPP Bureau - December 06, 2022

It offers quick relief in various types of Coughs, Colds and Sore Throat,

Lonza’s API manufacturing facility expansion in Nansha starts commercial operation
Lonza’s API manufacturing facility expansion in Nansha starts commercial operation

By IPP Bureau - December 06, 2022

Expanded capacity in Nansha, China will support mid-scale manufacturing to ensure a smooth transition between early-phase and large-scale commercial production

Agilent opens customer experience center for genomics and diagnostics solutions
Agilent opens customer experience center for genomics and diagnostics solutions

By IPP Bureau - December 06, 2022

New Lexington, Massachusetts facility to provide customer education and collaboration opportunities

Zydus receives final approval from USFDA for Estradiol Transdermal System
Zydus receives final approval from USFDA for Estradiol Transdermal System

By IPP Bureau - December 05, 2022

The drug will be manufactured at the group’s formulation manufacturing facility at Moraiya, Ahmedabad

Mirati Therapeutics announces update for the Phase 3 SAPPHIRE study
Mirati Therapeutics announces update for the Phase 3 SAPPHIRE study

By IPP Bureau - December 05, 2022

Evaluating Investigational Sitravatinib in combination with Nivolumab for patients with non-squamous non-small cell lung cancer

Valneva and Pfizer report antibody persistence data for lyme disease vaccine candidate
Valneva and Pfizer report antibody persistence data for lyme disease vaccine candidate

By IPP Bureau - December 05, 2022

Antibody levels remained above baseline six months after completion of a three-dose (Month 0-2-6) or a two-dose (Month 0-6) vaccination schedule

Merck to present data from Its hematology portfolio ASH meeting
Merck to present data from Its hematology portfolio ASH meeting

By IPP Bureau - December 05, 2022

Presentations include new data on investigational medicines – favezelimab (MK-4280), zilovertamab vedotin (MK-2140) and nemtabrutinib – as well as KEYTRUDA (pembrolizumab) in multiple blood cancers

Jemperli RUBY phase III trial met its primary endpoint
Jemperli RUBY phase III trial met its primary endpoint

By IPP Bureau - December 05, 2022

Results showed a statistically significant and clinically meaningful improvement in investigator-assessed progression-free survival

EMA accepts marketing authorisation application for momelotinib for the treatment of myelofibrosis
EMA accepts marketing authorisation application for momelotinib for the treatment of myelofibrosis

By IPP Bureau - December 05, 2022

Application includes data from key phase III trials, including the pivotal MOMENTUM trial, which met all primary and key secondary efficacy endpoints

World’s first intra-nasal vaccine for COVID developed by India has got approval from CDSCO
World’s first intra-nasal vaccine for COVID developed by India has got approval from CDSCO

By IPP Bureau - December 02, 2022

Phase-III trials were conducted for safety, and immunogenicity in around 3,100 subjects, in 14 trial sites across India (supported by BIRAC)

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