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  • abbvie news

Tag: abbvie news

You Searched For "abbvie news"
Premarket approval application for Skinvive by Juvederm for neck lines reduction under USFDA review: Abbvie Allergan Aesthetics

CVS Health to remove AbbVie rheumatoid arthritis drug Humira from some drug reimbursement lists in April

Ruchika Sharma4 Jan 2024 12:30 PM IST
A CVS spokesperson said the company expects most of its customers to transition their coverage to biosimilars of Humira, known chemically as...
AbbVie completes acquisition of Capstan Therapeutics

AbbVie to focus on smaller deals after buying spree

Ruchika Sharma9 Dec 2023 2:30 PM IST
AbbVie said it expects to return to "robust growth" in 2025, after its recent buying spree.
Premarket approval application for Skinvive by Juvederm for neck lines reduction under USFDA review: Abbvie Allergan Aesthetics

AbbVie to acquire Cerevel Therapeutics for USD 8.7 billion

Ruchika Sharma8 Dec 2023 12:30 PM IST
North Chicago: AbbVie Inc. and Cerevel Therapeutics have announced a definitive agreement under which AbbVie will acquire Cerevel Therapeutics and its...
Boehringer unveils 81 percent discounted biosimilar of AbbVie Humira

Boehringer unveils 81 percent discounted biosimilar of AbbVie Humira

Ruchika Sharma4 Oct 2023 3:30 PM IST
Until recently, Humira was the world's biggest-selling prescription drug. It had sales of USD 21.2 billion in 2022.
AbbVie completes acquisition of Capstan Therapeutics

AbbVie blood cancer combo therapy fails in late-stage study

Ruchika Sharma2 Oct 2023 1:00 PM IST
United States: AbbVie has said a late-stage study of its experimental combination therapy to treat a form of blood cancer failed to meaningfully...
AbbVie gets European Commission nod for Aquipta for prophylaxis of migraine in adults

AbbVie gets European Commission nod for Aquipta for prophylaxis of migraine in adults

Ruchika Sharma20 Aug 2023 3:00 PM IST
North Chicago: AbbVie has announced that the European Commission has approved AQUIPTA (atogepant) for the prophylaxis of migraine in adults...
Lupin Gets Expert Committee Nod To Conduct Phase I Trial of Certolizumab Pegol, IGRA TB Test Made Mandatory

Lupin receives over Rs 205 crore from AbbVie for meeting key product development milestone

Ruchika Sharma30 Jun 2023 2:00 PM IST
Mumbai: Global pharma major Lupin Limited has announced the achievement of a key milestone for its novel MALT1 (Mucosa-Associated Lymphoid Tissue ...
Coherus resolves part of dispute with AbbVie over Humira biosimilar

Coherus resolves part of dispute with AbbVie over Humira biosimilar

Ruchika Sharma17 Jun 2023 11:00 AM IST
Coherus BioSciences said on Thursday it had agreed to retract a restraining order against AbbVie as the two fight over the terms of launching a...
AbbVie gets USFDA nod for EPKINLY to treat adult patients with relapsed or refractory Diffuse Large B-Cell Lymphoma

AbbVie gets USFDA nod for EPKINLY to treat adult patients with relapsed or refractory Diffuse Large B-Cell Lymphoma

Ruchika Sharma20 May 2023 11:30 AM IST
DLBCL is a type of aggressive, fast-growing non-Hodgkin's lymphoma, a cancer that develops in the lymphatic system and affects B cells, a type of...
AbbVie completes acquisition of Capstan Therapeutics

AbbVie plan to withdraw accelerated nods of Imbruvica in US for patients with certain types of blood cancer

Ruchika Sharma7 April 2023 3:30 PM IST
IMBRUVICA is jointly developed and commercialized by Pharmacyclics LLC, an AbbVie company and Janssen Biotech, Inc.
AbbVie completes acquisition of Capstan Therapeutics

AbbVie trims profit forecasts on IPRnD expenses

Ruchika Sharma7 April 2023 2:30 PM IST
United States: AbbVie Inc has lowered its full-year and first-quarter profit expectations, citing a $150 million hit from acquired in-process...
USFDA refuses to approve AbbVie Parkinsons disease therapy ABBV-951, seeks more information

USFDA refuses to approve AbbVie Parkinson's disease therapy ABBV-951, seeks more information

Ruchika Sharma23 March 2023 12:15 PM IST
The US health regulator has not sought additional efficacy and safety trials, the company said, adding it plans to resubmit the marketing application...
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