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August 04, 2017

Today's Rundown

  1. Bristol-Myers Squibb in $2.3B I-O biotech biobucks buyout deal

  2. Senate passes FDA user fee and right-to-try bills

  3. Aeterna accuses ex-CEO of secret plot to buy lead asset

  4. Lilly plans 2018 filing for acute migraine drug after second phase 3 win

  5. Veritas buys Curoverse to boost genomic data capabilities

  6. AbbVie's new pan-genotypic hepatitis C drug Mavyret deeply underprices the competition

  7. EuroBiotech Report—Idorsia insomnia data, Chiesi-uniQure, Redx-Loxo, Servier-Galapagos and Intec cannabinoid data

  8. FiercePharmaAsia—GSK’s neurology R&D hub, Pfizer-Astellas’ aborted Xtandi mission, Daiichi Sankyo’s Benicar settlement

  9. Chutes & Ladders—Biogen poaches Pfizer executive as medicinal sciences head

Featured Story

Bristol-Myers Squibb in $2.3B I-O biotech biobucks buyout deal

Bristol-Myers Squibb will pay $300 million upfront and up to $2 billion in biobucks for IFM Therapeutics and its new immuno-oncology approaches.

Top Stories

Senate passes FDA user fee and right-to-try bills

The Senate has voted in quick succession to pass bills reauthorizing the FDA to collect fees from the industry and expanding access to unapproved medicines. President Trump is now set to sign the user fee bill into law, while the right-to-try legislation will go to the House.

Aeterna accuses ex-CEO of secret plot to buy lead asset

Aeterna Zentaris has accused its former CEO and general counsel of plotting secretly to buy its lead candidate. The tiny, floundering biotech made the claim in a statement disclosing legal action it has begun against the pair over alleged disclosures of confidential information.

Lilly plans 2018 filing for acute migraine drug after second phase 3 win

Eli Lilly's bid to bring a new class of migraine therapy to market has just been lifted by a second positive trial that sets up first-marketing applications next year.

Veritas buys Curoverse to boost genomic data capabilities

Veritas Genetics has bought Curoverse to dial up its genome data interpretation capabilities. The takeover combines two George Church, Ph.D., cofounded startups to create a company equipped to sequence and make sense of genomes at scale.

AbbVie's new pan-genotypic hepatitis C drug Mavyret deeply underprices the competition

Get set for even more competition in the hepatitis C space. AbbVie’s Mavyret picked up FDA approval on Thursday as an eight-week treatment regardless of genotype, becoming the first such drug with the indication.

EuroBiotech Report—Idorsia insomnia data, Chiesi-uniQure, Redx-Loxo, Servier-Galapagos and Intec cannabinoid data

In this week's EuroBiotech Report, Idorsia posts insomnia data, Chiesi dumps uniQure, Loxo buys Redx drug and more. 

FiercePharmaAsia—GSK’s neurology R&D hub, Pfizer-Astellas’ aborted Xtandi mission, Daiichi Sankyo’s Benicar settlement

GlaxoSmithKline will soon close its global neuroscience R&D hub located in Shanghai, Pfizer and Astellas have decided to discontinue research into Xtandi's usage in breast cancer, Daiichi Sankyo is offering $300 million to settle about 2,300 lawsuits around Benicar and other news items from Asia's pharma industry.

Chutes & Ladders—Biogen poaches Pfizer executive as medicinal sciences head

Biogen poached Pfizer executive Villalobos to lead its medicinal sciences efforts, AstraZeneca made two new oncology hires after the Mystic fall, Moderna tapped an industry veteran previously with Novartis to oversee manufacturing. Plus more hirings, firings and retirings throughout the industry.

Resources

[Webinar] Results from the 2017 Unified Clinical Operations Survey

Learn why 99% of respondents report the need to unify their clinical applications, including CTMS, EDC, eTMF, and study start-up.

[Video] API Discussion with Dr. Robert DeWit, CEO of MPI Research

FierceBiotech interviews Dr. DeWit to discuss a common cause for drug development delays, and strategies to avoid these costly setbacks.

[Whitepaper] Industry Report: Findings from the 2017 Unified Clinical Operations Survey

Learn why 99% of respondents report the need to unify their clinical applications, including CTMS, EDC, eTMF, and study start-up.

[Webinar] Within-Subject Clinical Trials: Intro to New Methods & Stat. Models

In this webinar, we will introduce the rapidly-evolving within-subject clinical trial (WSCT) methods for early phase evidence generation that require fewer people, less time, and usually less funding than traditional early phase methods.

[Webinar] Leveraging Medical Insights for Better Healthcare Engagement

Join this global webinar to learn a new approach for demonstrating medical affairs' impact with better metrics - beyond reach and frequency, enabling launch success and better engagement with strategic KOL insights, and increasing your organization's share of voice in the healthcare landscape.

Events

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