IPP Bureau

GlaxoSmithKline Pharmaceuticals appoints GoApptiv as super stockist
GlaxoSmithKline Pharmaceuticals appoints GoApptiv as super stockist

By IPP Bureau - June 25, 2024

This tie-up will have no impact on any other brands of the company

Venus Remedies clinches WHO-backed PAHO tender
Venus Remedies clinches WHO-backed PAHO tender

By IPP Bureau - June 25, 2024

The company has been entrusted with the responsibility of supplying a wide range of essential oncology drugs

Sun Pharma’s Utreglutide demonstrates significant weight loss at the American Diabetes Association 84th Scientific Sessions
Sun Pharma’s Utreglutide demonstrates significant weight loss at the American Diabetes Association 84th Scientific Sessions

By IPP Bureau - June 25, 2024

GL0034 administered once-weekly confirmed clinically meaningful weight loss and improved glucometabolic parameters over a 4-week treatment period in individuals with obesity

Sun Pharma completes Taro merger
Sun Pharma completes Taro merger

By IPP Bureau - June 25, 2024

Combined entity is better positioned to compete in increasingly competitive generics industry

Arkema grants technology license to Seqens to manufacture PEKK for sale in medical implantable applications
Arkema grants technology license to Seqens to manufacture PEKK for sale in medical implantable applications

By IPP Bureau - June 25, 2024

PEKK is a high-performance polymer family used in aerospace and other demanding markets

Ascentage Pharma closes US$ 75 million equity investment by Takeda
Ascentage Pharma closes US$ 75 million equity investment by Takeda

By IPP Bureau - June 24, 2024

Ascentage Pharma announces confidential submission of draft registration statement for proposed IPO

MediPharm Labs acquires advanced medical cannabis delivery method technology from Remidose Aerosols
MediPharm Labs acquires advanced medical cannabis delivery method technology from Remidose Aerosols

By IPP Bureau - June 24, 2024

Transaction is non-dilutive, with 100% performance-based payment through a royalty model

EMA approves Biocon Biologics’ new mAbs facility in India
EMA approves Biocon Biologics’ new mAbs facility in India

By IPP Bureau - June 24, 2024

Renews GMP certifications for India and Malaysia sites

CCRAS to organize national consultative meet on ‘Research Priority Settings in Traditional Medicine’ in collaboration with WHO
CCRAS to organize national consultative meet on ‘Research Priority Settings in Traditional Medicine’ in collaboration with WHO

By IPP Bureau - June 24, 2024

The consultative meet, a first of its kind, will bring together representatives from diverse domains of Traditional Medicine (TM) in India

Cipla gets 6 observations from USFDA for Goa facility
Cipla gets 6 observations from USFDA for Goa facility

By IPP Bureau - June 24, 2024

The company will work closely with the USFDA and is committed to address these comprehensively within stipulated time

Ami Organics raises Rs. 400 crores through QIP
Ami Organics raises Rs. 400 crores through QIP

By IPP Bureau - June 24, 2024

The Issue opened on June 18, 2024 and closed on June 21, 2024

AstraZeneca Pharma India updates on exploring contract manufacturer
AstraZeneca Pharma India updates on exploring contract manufacturer

By IPP Bureau - June 24, 2024

The company will now explore a buyer for its manufacturing site and exit in due course

Truqap plus Faslodex approved in the EU for patients with advanced ER-positive breast cancer
Truqap plus Faslodex approved in the EU for patients with advanced ER-positive breast cancer

By IPP Bureau - June 22, 2024

Approval based on CAPItello-291 results which showed this combination reduced the risk of disease progression or death by 50% vs. Faslodex alone in a biomarker-altered population

AbbVie appoints Roxanne S. Austin as Lead Independent Director of the Board of Directors
AbbVie appoints Roxanne S. Austin as Lead Independent Director of the Board of Directors

By IPP Bureau - June 22, 2024

Austin assumes role from Glenn F. Tilton, who will continue to serve as an independent director

Bristol Myers Squibb receives USFDA accelerated approval of Krazati in combination with Cetuximab for CRC
Bristol Myers Squibb receives USFDA accelerated approval of Krazati in combination with Cetuximab for CRC

By IPP Bureau - June 22, 2024

Second FDA approval for KRAZATI - reinforcing its potential across tumor types

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