IPP Bureau

Lupin secures SBTi validation for emission reduction targets
Lupin secures SBTi validation for emission reduction targets

By IPP Bureau - December 17, 2025

Glenmark secures exclusive multi-regional rights to Aumolertinib from Hansoh Pharma
Glenmark secures exclusive multi-regional rights to Aumolertinib from Hansoh Pharma

By IPP Bureau - December 17, 2025

Hansoh Pharma will receive an upfront payment in the low double-digit millions

Remedium Lifecare is now Supha Pharmachem
Remedium Lifecare is now Supha Pharmachem

By IPP Bureau - December 17, 2025

The company shall process the change of name application with BSE Ltd. in due course

Lupin receives EIR from USFDA for Nagpur injectable facility
Lupin receives EIR from USFDA for Nagpur injectable facility

By IPP Bureau - December 17, 2025

The EIR was issued following an inspection of the facility from September 8 to September 16, 2025

AstraZeneca wins EU nod for self-administered lupus drug Saphnelo
AstraZeneca wins EU nod for self-administered lupus drug Saphnelo

By IPP Bureau - December 17, 2025

Convenient subcutaneous option has potential to reach more patients with same clinical benefits as Saphnelo IV infusion

Cynata completes patient enrollment for Phase 2 aGvHD clinical trial
Cynata completes patient enrollment for Phase 2 aGvHD clinical trial

By IPP Bureau - December 17, 2025

Patient enrolment has been completed in Cynata's Phase 2 clinical trial of CYP-001 in acute graft versus host disease

Bristol Myers Squibb launches AI-powered ‘Mosaic’ hub in Mumbai
Bristol Myers Squibb launches AI-powered ‘Mosaic’ hub in Mumbai

By IPP Bureau - December 17, 2025

India plays a critical role in Bristol Myers Squibb’s global strategy

Revvity unveils AI-powered Signals Xynthetica to accelerate molecular and materials design
Revvity unveils AI-powered Signals Xynthetica to accelerate molecular and materials design

By IPP Bureau - December 17, 2025

The Signals Xynthetica solution brings AI-driven in-silico generation, predictive modeling, and experimental validation into a single, governed environment

Merck KGaA launches ChemiSphere App to digitize lab workflows
Merck KGaA launches ChemiSphere App to digitize lab workflows

By IPP Bureau - December 17, 2025

The ChemiSphere app exemplifies how M-Trust technology transforms workflows into seamless digital experiences

Pfizer cuts 2026 revenue outlook amid COVID-19 & patent losses
Pfizer cuts 2026 revenue outlook amid COVID-19 & patent losses

By IPP Bureau - December 17, 2025

The pharmaceutical giant now expects 2026 revenues to land between $59.5 billion and $62.5 billion

Gujarat Kidney and Super Speciality to file IPO at Rs.108- Rs.114 per share
Gujarat Kidney and Super Speciality to file IPO at Rs.108- Rs.114 per share

By IPP Bureau - December 17, 2025

The company operates a chain of mid-sized multi-speciality hospitals

Minghui Pharmaceutical gets FDA green light for Phase III trials of its therapy in thyroid eye disease
Minghui Pharmaceutical gets FDA green light for Phase III trials of its therapy in thyroid eye disease

By IPP Bureau - December 17, 2025

The upcoming trials will evaluate both active and chronic TED in randomized, double-blind, placebo-controlled studies

Ascletis Pharma reports positive Phase I results for oral IL-17 inhibitor
Ascletis Pharma reports positive Phase I results for oral IL-17 inhibitor

By IPP Bureau - December 17, 2025

The randomized, double-blind, placebo-controlled single ascending dose (SAD) study evaluated safety, tolerability, pharmacokinetics, and target engagement in 46 healthy participants

Vanda Pharmaceuticals seeks FDA nod for breakthrough psoriasis drug
Vanda Pharmaceuticals seeks FDA nod for breakthrough psoriasis drug

By IPP Bureau - December 17, 2025

Imsidolimab, an IgG4 IL-36 receptor antagonist, works by inhibiting IL-36 receptor signaling, directly addressing the deficiency in the IL-36RA regulator common in GPP patients

FDA nod to first oral single-dose treatment for gonorrhea
FDA nod to first oral single-dose treatment for gonorrhea

By IPP Bureau - December 16, 2025

The approval of Nuzolvence (zoliflodacin) follows a collaborative development effort with the Global Antibiotic Research and Development Partnership

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