IPP Bureau

GenSci launches global innovation hub in Shanghai
GenSci launches global innovation hub in Shanghai

By IPP Bureau - December 26, 2023

The establishment of the facility demonstrates the company's commitment to delivering differentiated solutions to gynecology and pediatrics challenges

AstraZeneca to acquire China's Gracell Biotechnologies for US $1.2 billion
AstraZeneca to acquire China's Gracell Biotechnologies for US $1.2 billion

By IPP Bureau - December 26, 2023

Furthering cell therapy ambition across oncology and autoimmune diseases

Roche receives USFDA’s priority review to Xolair for food allergies based on positive NIH Phase III study results
Roche receives USFDA’s priority review to Xolair for food allergies based on positive NIH Phase III study results

By IPP Bureau - December 26, 2023

If approved, Xolair would be the first medicine to reduce allergic reactions to multiple foods following an accidental exposure

Wainua granted first-ever regulatory approval in the US for improving neuropathy impairment
Wainua granted first-ever regulatory approval in the US for improving neuropathy impairment

By IPP Bureau - December 26, 2023

US FDA approval based on NEURO-TTRansform Phase III results

BioVaxys executes LoI for major Immunotherapeutics technology acquisition
BioVaxys executes LoI for major Immunotherapeutics technology acquisition

By IPP Bureau - December 26, 2023

BioVaxys has been granted exclusivity while the parties work in good faith on the drafting of a definitive agreement

Astellas completes acquisition of Propella Therapeutics
Astellas completes acquisition of Propella Therapeutics

By IPP Bureau - December 26, 2023

Astellas has acquired abiraterone decanoate being developed by Propella to treat prostate cancer

Eugia's East Windsor facility gets 10 observations from USFDA
Eugia's East Windsor facility gets 10 observations from USFDA

By IPP Bureau - December 25, 2023

The plant is yet to start commercial operations

Stelis Biopharma updates on receipt of consideration from Syngene
Stelis Biopharma updates on receipt of consideration from Syngene

By IPP Bureau - December 25, 2023

Syngene has completed a payment of Rs. 158.2 crores on December 22, 2023 in addition to the initial payment of Rs. 395 crores made on December 1, 2023

Ind-Swift Laboratories receives award from World HRD Congress
Ind-Swift Laboratories receives award from World HRD Congress

By IPP Bureau - December 25, 2023

World HRD Congress is a well-known international body of Management Studies

Lyndra Therapeutics raises US$101 million in Series E funding
Lyndra Therapeutics raises US$101 million in Series E funding

By IPP Bureau - December 25, 2023

Funding round led by Sarissa Capital, includes Sun Pharma, Polaris Partners

Bristol Myers Squibb to buy Karuna Therapeutics for US$ 14 billion
Bristol Myers Squibb to buy Karuna Therapeutics for US$ 14 billion

By IPP Bureau - December 24, 2023

Transaction delivers KarXT, a first-in-class M1/ M4 muscarinic receptor agonist with differentiated efficacy and safety

Biocon Biologics signs distribution partnership with Sandoz for Adalimumab BS Subcutaneous Injection in Japan
Biocon Biologics signs distribution partnership with Sandoz for Adalimumab BS Subcutaneous Injection in Japan

By IPP Bureau - December 23, 2023

The transfer of the distribution rights will strengthen Sandoz's immunology and biosimilar portfolio

Zydus Lifesciences' API site in Ahmedabad. receives 6 observations from USFDA
Zydus Lifesciences' API site in Ahmedabad. receives 6 observations from USFDA

By IPP Bureau - December 23, 2023

This PAI-cum-GMP USFDA inspection was conducted from December 14 to December 22, 2023

Lupin Atlantis Holdings to acquire accretive established products in Europe and Canada from Sanofi
Lupin Atlantis Holdings to acquire accretive established products in Europe and Canada from Sanofi

By IPP Bureau - December 23, 2023

The brands Aarne in Germany and Nalcrom in Canada and the Netherlands are being acquired

USFDA grants priority review for Patritumab Deruxtecan in US for certain patients with EGFR-mutated non-small cell lung cancer
USFDA grants priority review for Patritumab Deruxtecan in US for certain patients with EGFR-mutated non-small cell lung cancer

By IPP Bureau - December 23, 2023

If approved, patritumab deruxtecan would be a first-in-class HER3 directed DXd antibody drug conjugate for these patients

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