IPP Bureau

SRL Diagnostics opens state-of-the-art laboratory in Jamshedpur
SRL Diagnostics opens state-of-the-art laboratory in Jamshedpur

By IPP Bureau - April 26, 2022

The new lab in the industrial town is SRL’s 4th lab in the state of Jharkhand

Sygnature Discovery acquires Peak Proteins
Sygnature Discovery acquires Peak Proteins

By IPP Bureau - April 26, 2022

Peak Proteins has collaborated closely with Sygnature Discovery for several years and together the companies have supported a number of integrated drug discovery programmes

GSK launches once daily, single inhaler-triple therapy for COPD patients
GSK launches once daily, single inhaler-triple therapy for COPD patients

By IPP Bureau - April 26, 2022

Trelegy is delivered via the innovative Ellipta inhaler that provides accurate dosing through its consistent dose delivery mechanism and is associated with less inhaler teaching time compared to other commonly used inhalers

Differentiation based on innovation is the way forward: S Aparna
Differentiation based on innovation is the way forward: S Aparna

By IPP Bureau - April 26, 2022

Secretary, Department of Pharmaceuticals and Union Health Secretary Chair a Panel Discussion on the theme 'Indian Pharma Vision 2047'

Drugs Controller clears Covaxin, Corbevax and ZyCov-D for kids
Drugs Controller clears Covaxin, Corbevax and ZyCov-D for kids

By IPP Bureau - April 26, 2022

The approval by the DCGI comes following recommendations by the Subject Expert Committee (SEC) on Covid-19 of the Central Drugs Standard Control Organisation(CDSCO)

Corbevax gets DCGI nod for Emergency Use in 5-12 years
Corbevax gets DCGI nod for Emergency Use in 5-12 years

By IPP Bureau - April 26, 2022

The approval comes soon after Corbevax was given the nod for 12-15-year group

DCGI grants Covaxin Emergency Use Approval for children 6-12 years
DCGI grants Covaxin Emergency Use Approval for children 6-12 years

By IPP Bureau - April 26, 2022

Covaxin was earlier approved for children 12-18 years of age

ZyCoV-D two-dose vaccine receives Emergency Use Approval from DCGI
ZyCoV-D two-dose vaccine receives Emergency Use Approval from DCGI

By IPP Bureau - April 26, 2022

The two-dose regimen for ZyCoV-D was tested in 3100 healthy volunteers more than 12 years of age

Bachem partners with Eli Lilly on oligonucleotide-based APIs
Bachem partners with Eli Lilly on oligonucleotide-based APIs

By IPP Bureau - April 26, 2022

Under the terms of the agreement, Bachem will provide the appropriate engineering infrastructure and expertise to implement Lilly’s novel oligonucleotide manufacturing technology

CanSinoBIO rebrands to reflect commitment to life sciences research
CanSinoBIO rebrands to reflect commitment to life sciences research

By IPP Bureau - April 25, 2022

This is the first major brand refresh of CanSinoBIO since its inception in 2009

Global AYUSH meet ends with promise of Rs 9000 cr. in investment
Global AYUSH meet ends with promise of Rs 9000 cr. in investment

By IPP Bureau - April 25, 2022

Investment and innovation opportunities in the field of AYUSH are limitless : Sarbananda Sonowal

Shionogi’s once-a-day Covid-19 anti-viral shows rapid virus clearance
Shionogi’s once-a-day Covid-19 anti-viral shows rapid virus clearance

By IPP Bureau - April 25, 2022

A separate global Phase 3 study of S-217622 is underway aiming to recruit participants globally to support regulatory filings this year

‘DREAM-ND’ and ‘DREAM-D’ Phase 3 trials of Desidustat published in American Journal of Nephrology
‘DREAM-ND’ and ‘DREAM-D’ Phase 3 trials of Desidustat published in American Journal of Nephrology

By IPP Bureau - April 25, 2022

Desidustat is currently approved only in India as OxemiaTM for patients with CKD induced anemia

Glenmark is the first to launch Teneligliptin and Pioglitazone Fixed-Dose Combination
Glenmark is the first to launch Teneligliptin and Pioglitazone Fixed-Dose Combination

By IPP Bureau - April 25, 2022

The innovative Fixed-Dose Combination will help improving the glycemic control among adult patients with insulin resistance, those whose diabetes is uncontrolled by metformin; and also those who require addition of Teneliglitptin and Pioglitazone as separate drugs.

Aleor Dermaceuticals receives USFDA approval for Clobestasol
Aleor Dermaceuticals receives USFDA approval for Clobestasol

By IPP Bureau - April 25, 2022

Clobetasol Propionate Foam, 0.05% has an estimated market size of US $ IO million for twelve months ending Dec 2021 according to IQVIA

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