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BioWorld - Sunday, March 22, 2026
Home » Novartis AG

Articles Tagged with ''Novartis AG''

Optogenetics illustration

Novartis sees the light, acquiring Vedere for $280M

Oct. 29, 2020
By Lee Landenberger
Novartis AG is expanding its position in the optogenetics space with the acquisition of Vedere Bio Inc., bringing with it a program aimed at vision loss prevention and treatment. Shareholders of Vedere, created in June 2019 through the Atlas Venture incubator, received $150 million up front and are eligible for up to $130 million in milestone payments, bringing the total to $280 million.
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Lilly antibody quality testing process
Potential paydays

Lilly, Novartis continue to push ahead with COVID-19 efforts

Oct. 28, 2020
By Michael Fitzhugh
With the world heading straight into a "very tough" stretch of the COVID-19 pandemic in which "too many countries are seeing an exponential increase in cases," according to World Health Organization Director-General Tedros Adhanom Ghebreyesus, two lucrative deals announced Oct. 28 showed little slack in efforts to confront the virus, even as evidence is still developing.
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Acute myeloid leukemia illustration

Priothera closes $35M series A round for pivotal trial to boost HSCT outcomes in AML

Oct. 12, 2020
By Cormac Sheridan
DUBLIN – Priothera Ltd. closed a €30 million (US$35.4 million) series A round to shepherd an oral sphingosine 1 phosphate (S1P) receptor agonist through clinical development in patients with acute myeloid leukemia (AML) who are undergoing allogeneic hematopoietic stem cell transplantation (HSCT).
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Prescription drug bottle, pills shaped in $ sign

Congressional Klieg lights could give way to restructuring of biopharma

Oct. 1, 2020
By Mari Serebrov
Attributing recent reductions in certain U.S. prescription drug prices to intense congressional scrutiny rather than a biopharma industry commitment to affordability, Rep. John Sarbanes (D-Md.) said Congress must put more guardrails in place and restructure how the industry does business.
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Rx pricing hearing highlights U.S. policy divide, gaps in understanding

Sep. 30, 2020
By Mari Serebrov
Rather than the in-your-face, blame-and-shame show that was expected, the Sept. 30 drug pricing hearing before the U.S. House Oversight Committee was more a reminder of the policy differences between Democrats and Republicans on how best to make prescription drugs more affordable.
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AI silhouette

Bioplus Interphex Korea: Novartis optimistic about future with AI

Sep. 29, 2020
By Gina Lee
HONG KONG – Novartis AG was cited during the recent 2020 KoNECT-MOHW-MFDS International Conference as an example of a biopharma firm staying ahead of the artificial intelligence curve.
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AI silhouette

Bioplus Interphex Korea: Novartis optimistic about future with AI

Sep. 25, 2020
By Gina Lee
HONG KONG – Novartis AG was cited during the recent 2020 KoNECT-MOHW-MFDS International Conference as an example of a biopharma firm staying ahead of the artificial intelligence curve. During this week’s 2020 Bioplus Interphex Korea conference, Won Kim, head of innovation at Novartis Korea, described some of the firm’s latest forays into AI, including negotiations with potential partners to develop an AI image analysis solution for retinal diseases.
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Biopharma companies draw ire for stepping into 340B oversight void

Sep. 16, 2020
By Mari Serebrov
Given the minimal accountability written into the 340B prescription drug discount program, a few biopharma companies recently began taking oversight into their own hands by demanding data claims or refusing to extend the mandated discounts to contract pharmacies.
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Novartis' anti-PD1 spartalizumab falls short in phase III melanoma trial

Aug. 24, 2020
By Michael Fitzhugh
A phase III study evaluating a combination of a Novartis AG anti-PD-1 candidate with the well-established BRAF/MEK inhibitor combo in first-line unresectable or metastatic BRAF V600 mutant melanoma missed its primary endpoint of progression-free survival.
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FDA Approved stamp

New pen pal? Novartis’ Kesimpta greenlighted in relapsing MS with autoinjector

Aug. 20, 2020
By Randy Osborne
Novartis AG won FDA clearance for the anti-CD20 monoclonal antibody Kesimpta (ofatumumab) in relapsing forms of multiple sclerosis (MS) in adults, with a label that includes clinically isolated syndrome and relapsing-remitting as well as active secondary progressive disease.
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