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BioWorld - Tuesday, April 21, 2026
Home » Topics » Drugs

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NS Pharma’s Viltepso cleared to take on troubled DMD drug Vyondys

Aug. 12, 2020
By Jennifer Boggs
The FDA granted accelerated approval to Viltepso (viltolarsen) to treat Duchenne muscular dystrophy patients (DMD) who have a confirmed mutation of the DMD gene amenable to exon 53 skipping, pitting it against Sarepta Therapeutics Inc.’s Vyondys (golodirsen), which was given accelerated approval last year in a controversial decision by the FDA following an agency complete response letter (CRL) highlighting safety concerns.
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Pakistan flag-map

Import bans hit Pakistan’s pharma industry

Aug. 11, 2020
By Khawar Khan
KARACHI, Pakistan – Geopolitics and a fraught relationship with its neighbors are hurting Pakistan’s pharmaceutical industry and the ability of people to access active pharmaceutical ingredients (APIs) and modern drugs.
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U.S. flag and White House podium
On the campaign trail

Trump promises to bring drug supply chain home

Aug. 11, 2020
By Mari Serebrov
With the economy and public health on the line, U.S. President Donald Trump thumped his Made in America pulpit again Thursday on a campaign swing through Ohio, in which he vowed to bring the pharmaceutical supply chain home over the next four years.
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Pakistan flag-map

Import bans hit Pakistan’s pharma industry

Aug. 7, 2020
By Khawar Khan
KARACHI, Pakistan – Geopolitics and a fraught relationship with its neighbors are hurting Pakistan’s pharmaceutical industry and the ability of people to access active pharmaceutical ingredients (APIs) and modern drugs.
Read More

Bayer’s Lampit approved by FDA to treat Chagas disease

Aug. 7, 2020
By Lee Landenberger
U.S. flag and White House podium
On the campaign trail

Trump promises to bring drug supply chain home

Aug. 6, 2020
By Mari Serebrov
With the economy and public health on the line, U.S. President Donald Trump thumped his Made in America pulpit again Thursday on a campaign swing through Ohio, in which he vowed to bring the pharmaceutical supply chain home over the next four years.
Read More

FDA clears GSK’s Blenrep in multiple myeloma; black box and REMS for eye tox

Aug. 6, 2020
By Randy Osborne
About two weeks after European regulators gave their go-ahead for Blenrep (belantamab mafodotin-blmf), the B cell maturation antigen (BCMA)-targeting therapy from Glaxosmithkline plc (GSK) for relapsed/refractory multiple myeloma (MM), the FDA did likewise.
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Marchin’ tune crescendoes as state AGs blast remdesivir price, supply

Aug. 5, 2020
By Mari Serebrov
Citing the limited supplies and the pricing of the COVID-19 therapy, nearly three dozen U.S. states and territories are clamoring for the federal government to march in on Gilead Sciences Inc.’s patents for remdesivir. And if the feds won’t, then states should be given that authority, according to a letter sent Tuesday to the Department of Health and Human Services, the NIH and the FDA.
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Taiwan’s Senhwa advancing CK2 candidate against moderate COVID-19

Aug. 4, 2020
By Elise Mak
Senhwa Biosciences Inc., of Taipei, Taiwan, said casein kinase 2 (CK2) is the right target to aim at when developing a COVID-19 therapeutic treatment. The company’s silmitasertib is the only clinical-stage inhibitor of CK2, a kinase recently identified by researchers as being hijacked by SARS-CoV-2.
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Morphosys/Incyte/Xencor win FDA nod for Monjuvi in lymphoma

Aug. 3, 2020
By Nuala Moran
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