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BioWorld - Tuesday, January 13, 2026
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BioAsia 2020

India could be instrumental in lowering price of CAR T-cell therapy

Feb. 25, 2020
By T.V. Padma
HYDERABAD, India – India could play a key role in driving down the exorbitant cost of emerging cell and gene therapies, with a combination of comparatively cheap labor and efficient manufacturing, international experts said during the annual BioAsia conference.
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Pill bottle with flag of India
BioAsia 2020

India ramps up efforts to move up biotech value chain

Feb. 25, 2020
By T.V. Padma
HYDERABAD, India – Multinationals and domestic companies are stepping up research in India, including working to leverage the country’s digital and entrepreneurial capabilities, to boost India’s capabilities and market share in more innovative biologic drugs.
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Tablets on conveyor belt
Closer to home

Sanofi to launch new European API venture, citing industry’s heavy reliance on Asia

Feb. 25, 2020
By Michael Fitzhugh
Paris-based Sanofi SA, responding to increasing medicine shortages and drugmakers' heavy reliance on active pharmaceutical ingredients (APIs) sourced from Asia, said it plans to create a major new API manufacturer headquartered in France.
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Brain illustration

Lundbeck’s newly approved Vyepti enters a growth market for migraine prevention

Feb. 24, 2020
By Lee Landenberger
H. Lundbeck A/S’ antibody-based migraine therapy, Vyepti (eptinezumab-jjmr), which just received FDA approval as the first and only intravenous preventive treatment for adults, enters a market forecast to grow to $7 billion by 2027. While some analysts placed Vyepti’s earnings potential at about $800 million annually, the drug itself is positioned to become a possible blockbuster, earning $1 billion annually.
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NGM studios’ top-line phase II NASH premiere whets appetite for Alpine 2/3 sequel

Feb. 24, 2020
By Randy Osborne
NGM Biopharmaceuticals Inc. wowed investors with positive preliminary top-line results from the 24-week double-blind, randomized, placebo-controlled fourth cohort of an adaptive phase II study testing aldafermin in nonalcoholic steatohepatitis (NASH).
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Tablets on conveyor belt
Closer to home

Sanofi to launch new European API venture, citing industry’s heavy reliance on Asia

Feb. 24, 2020
By Michael Fitzhugh
Paris-based Sanofi SA, responding to increasing medicine shortages and drugmakers' heavy reliance on active pharmaceutical ingredients (APIs) sourced from Asia, said it plans to create a major new API manufacturer headquartered in France.
Read More

Esperion wins FDA approval for new cholesterol-lowering drug

Feb. 21, 2020
By Michael Fitzhugh
Less than a month after landing a positive opinion from the EMA's CHMP, Esperion Therapeutics Inc. has won FDA approval for bempedoic acid as an adjunct to diet and maximally tolerated statin therapy.
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FDA Approved road sign

Angle of ketorolac attack yakked as Baudax hails Anjeso pesos

Feb. 21, 2020
By Randy Osborne
During a conference call with investors, Baudax Bio Inc. CEO Gerri Henwood let out an exuberant “woohoo!” to celebrate the FDA’s approval – after two turndowns and much haggling over data – of Anjeso (meloxicam) for moderate to severe pain. Echoing her sentiment was Piper Sandler analyst David Amsellem. “It’s nice to see the pain division finally get this one right,” he said.
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BioAsia 2020

Digital strategies key for Indian pharma

Feb. 21, 2020
By T.V. Padma
HYDERABAD, India – To continue expanding their footprint and capabilities beyond simple generics to biosimilars and new chemical entities, Indian pharmaceutical companies will have to improve their quality controls, compliance capabilities and, just as importantly, adopt more effective digital strategies.
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Zelira’s medicinal cannabis therapy meets primary endpoints in phase I/II insomnia trial

Feb. 20, 2020
By Tamra Sami
PERTH, Australia – Medicinal cannabis company Zelira Therapeutics Ltd. reported that its ZLT-101 therapy met the primary endpoint of a statistically significant improvement in insomnia in a phase Ib/IIa study in patients diagnosed with chronic insomnia.
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