IPP Bureau

Wockhardt announces successful completion of pivotal Phase 3 pneumonia study of its macrolide antibiotic Nafithromycin WCK 4873
Wockhardt announces successful completion of pivotal Phase 3 pneumonia study of its macrolide antibiotic Nafithromycin WCK 4873

By IPP Bureau - December 12, 2023

The findings of Phase 3 study are in line with Phase 2 study conducted in the US and Europe

Briefs: GlaxoSmithKline Pharmaceuticals and Dr. Reddy's Laboratories
Briefs: GlaxoSmithKline Pharmaceuticals and Dr. Reddy's Laboratories

By IPP Bureau - December 10, 2023

Dr. Reddy's Laboratories has been issued a Form 483 with three observations

Pfizer presents marstacimab Phase 3 Data at ASH 2023
Pfizer presents marstacimab Phase 3 Data at ASH 2023

By IPP Bureau - December 10, 2023

Demonstrate significant bleed reduction in hemophilia A and B

Aptar Pharms opens new production facility at Taloja, Mumbai
Aptar Pharms opens new production facility at Taloja, Mumbai

By IPP Bureau - December 10, 2023

New facility is part of Aptar Pharma’s global expansion program

Astellas receives USFDA approval for expanded use of Cresemba for treatment of mucormycosis
Astellas receives USFDA approval for expanded use of Cresemba for treatment of mucormycosis

By IPP Bureau - December 10, 2023

Cresemba is the only azole antifungal therapy approved for pediatric patients as young as one affected by these serious, potentially life-threatening infections

ExeGi Pharma announces first patient enrollment in the PROF Trial of EXE-346
ExeGi Pharma announces first patient enrollment in the PROF Trial of EXE-346

By IPP Bureau - December 10, 2023

First published clinical trial using live biotherapeutic candidate in Covid-19 patients suggests role in improving outcomes

Max Healthcare acquires 550 bedded Sahara Hospital, Lucknow
Max Healthcare acquires 550 bedded Sahara Hospital, Lucknow

By IPP Bureau - December 09, 2023

This acquisition marks Max Healthcare's entry into Lucknow

Fire accident at Parmax Pharma’s plant
Fire accident at Parmax Pharma’s plant

By IPP Bureau - December 09, 2023

There has been no loss or injury to human life

European Commission approves Pfizer’s Elrexfio for multiple myeloma
European Commission approves Pfizer’s Elrexfio for multiple myeloma

By IPP Bureau - December 09, 2023

Conditional marketing authorization is based on clinically meaningful response rates, duration of response, and safety from the Phase 2 MagnetisMM-3 trial

Vertex and CRISPR Therapeutics announce USFDA approval of Casgevy for treatment of sickle cell disease
Vertex and CRISPR Therapeutics announce USFDA approval of Casgevy for treatment of sickle cell disease

By IPP Bureau - December 09, 2023

Approximately 16,000 patients 12 years of age and older with severe sickle cell disease may now be eligible for this one-time treatment

Zepbound is now available in US for adults living with obesity
Zepbound is now available in US for adults living with obesity

By IPP Bureau - December 09, 2023

Express Scripts to add Zepbound to National Preferred Formulary

Operations disrupted at NATCO Pharma's Manali, Chennai factory
Operations disrupted at NATCO Pharma's Manali, Chennai factory

By IPP Bureau - December 08, 2023

NATCO temporarily shut down the operations due to cyclone with flooding/water logging of the factory premises

TTK Healthcare halts operation at ortho implants plant at Ambattur
TTK Healthcare halts operation at ortho implants plant at Ambattur

By IPP Bureau - December 08, 2023

The company is assessing the situation and simultaneously undertaking all the requisite action

Sarclisa Phase 3 trial met primary endpoint of progression free survival with newly diagnosed multiple myeloma not eligible for transplant
Sarclisa Phase 3 trial met primary endpoint of progression free survival with newly diagnosed multiple myeloma not eligible for transplant

By IPP Bureau - December 08, 2023

Sarclisa added to bortezomib, lenalidomide and dexamethasone (VRd) significantly reduced the risk of disease progression or death compared with VRd alone

Novartis receives FDA approval for Fabhalta as the first oral monotherapy for adults with PNH
Novartis receives FDA approval for Fabhalta as the first oral monotherapy for adults with PNH

By IPP Bureau - December 08, 2023

Late-stage Fabhalta development program ongoing in multiple complement-mediated conditions

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