IPP Bureau

Finerenone showed statistically significant improvement in cardiovascular outcomes in adults with common form of heart failure
Finerenone showed statistically significant improvement in cardiovascular outcomes in adults with common form of heart failure

By IPP Bureau - September 02, 2024

Finerenone is the first mineralocorticoid receptor (MR) antagonist to demonstrate definitive cardiovascular benefits in a Phase III study in patients with heart failure (HF) with a left ventricular ejection fraction (LVEF) of ?40%

Merck announces first patient dosed in Phase III study of Oral Cladribine in gMG
Merck announces first patient dosed in Phase III study of Oral Cladribine in gMG

By IPP Bureau - September 02, 2024

MyClad is a global Phase III study evaluating the efficacy and safety of cladribine capsules for the treatment of generalized Myasthenia Gravis (gMG)

Govt. to improve availability of infrastructure and trained manpower for organ transplantation
Govt. to improve availability of infrastructure and trained manpower for organ transplantation

By IPP Bureau - September 01, 2024

Stressed was on the need to promote organ donation from the deceased persons to meet the huge need for organ donation in the country

Mitsubishi Chemical's clinical study demonstrates effectiveness of probiotic on intestinal environment
Mitsubishi Chemical's clinical study demonstrates effectiveness of probiotic on intestinal environment

By IPP Bureau - September 01, 2024

H.coagulans is, unlike other general lactobacillus, characterized by spore formation, giving it resistance to acid and heat

Biocon Pharma receives USFDA approval for daptomycin
Biocon Pharma receives USFDA approval for daptomycin

By IPP Bureau - September 01, 2024

The approval further adds to Biocon’s portfolio of complex drug products

Zydus receives warning letter from USFDA for Jarod injectables manufacturing facility
Zydus receives warning letter from USFDA for Jarod injectables manufacturing facility

By IPP Bureau - August 31, 2024

The company will take all necessary steps to work with USFDA towards earliest remediation of the above facility

Zydus receives USFDA final approval for Scopolamine Transdermal System 1 mg/3 days
Zydus receives USFDA final approval for Scopolamine Transdermal System 1 mg/3 days

By IPP Bureau - August 31, 2024

Thyrocare to acquire diagnostic and pathological services business of Vimta Labs
Thyrocare to acquire diagnostic and pathological services business of Vimta Labs

By IPP Bureau - August 31, 2024

Vimta Labs through its diagnostic and pathological services business has recorded a revenue of Rs. 30 crores during FY 2024 and Rs. 7 crores in Q1 FY 2025

DKSH partners with Hasten Biopharmaceutical’s growth in Thailand
DKSH partners with Hasten Biopharmaceutical’s growth in Thailand

By IPP Bureau - August 31, 2024

Indian doctor participates in Jordan’s first robotic radical hysterectomies
Indian doctor participates in Jordan’s first robotic radical hysterectomies

By IPP Bureau - August 31, 2024

Biocon Biologics secures market entry for Bmab 1200 in Europe, UK, Canada, and Japan
Biocon Biologics secures market entry for Bmab 1200 in Europe, UK, Canada, and Japan

By IPP Bureau - August 30, 2024

Biocon Biologics earlier announced a settlement agreement in the United States for a Bmab 1200 launch no later than February 22, 2025

Vaishali Pharma Ltd recommends 1:1 bonus issue and 1:5 stock split
Vaishali Pharma Ltd recommends 1:1 bonus issue and 1:5 stock split

By IPP Bureau - August 30, 2024

The company is making its mark through strategic initiatives, promising to become a significant presence in the evolving pharmaceutical sector

Natco Pharma announces submission of TABRECTA to USFDA
Natco Pharma announces submission of TABRECTA to USFDA

By IPP Bureau - August 30, 2024

TABRECTA is the brand of Novartis. Natco believes it is the first company to have filed a substantially-complete ANDA

Ayurvedic Whole System effective in Managing Rheumatoid Arthritis: Study
Ayurvedic Whole System effective in Managing Rheumatoid Arthritis: Study

By IPP Bureau - August 30, 2024

The study highlighted substantial improvements in key clinical parameters among RA patients who underwent AWS intervention

Suven Life Sciences announces FDA acceptance of investigational new drug
Suven Life Sciences announces FDA acceptance of investigational new drug

By IPP Bureau - August 30, 2024

First-in-human Phase-1 study will evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of SUVN-I6107 in healthy subjects

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