Biotech: Page 66


  • A photograph of Amylyx Pharmaceuticals cofounders Josh Cohen and Justin Klee.
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    Permission granted by Amylyx Pharmaceuticals
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    ALS drug development

    ALS drug approved by FDA in closely watched decision, marking win for patients, developer

    The drug, which will be sold as Relyvrio, showed modest benefits in function and survival in testing. It also became the latest test of the FDA's flexibility toward new therapies for neurological disorders.

    By Updated Sept. 30, 2022
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    Sudo joins a wave of startups taking aim at Bristol Myers’ new skin disease drug

    The startup, which emerged Wednesday with $37 million in funding, is the latest company trying to top Bristol Myers’ TYK2 inhibitor Sotyktu.

    By Sept. 28, 2022
  • Explore the Trendline
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    Spencer Platt via Getty Images
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    Trendline

    Emerging biotech

    New biotechs continue to emerge despite a challenging market environment that has forced venture firms to build their drug startups more cautiously.

    By BioPharma Dive staff
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    National Institute on Aging. (2017). "Beta-Amyloid Plaques and Tau in the Brain" [Image]. Retrieved from Flickr.
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    New Alzheimer's drugs

    In surprise result, Alzheimer’s drug from Eisai, Biogen shows benefit in large trial

    The companies’ drug lecanemab met all of its goals in the Phase 3 study. The data were a significant finding and provided stronger support for a much-debated hypothesis for treating Alzheimer’s.

    By Updated Sept. 27, 2022
  • A photo of Vertex Pharmaceuticals' Boston headquarters.
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    Courtesy of Vertex Pharmaceuticals
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    Vertex given green light to seek US approval of CRISPR-based therapy

    The company and its development partner, CRISPR Therapeutics, will begin submitting a rolling application in November. The blood disease treatment is the first of its kind to near an FDA review. 

    By Sept. 27, 2022
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    Courtesy of Scribe Therapeutics
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    Sanofi partners with Scribe to gain gene editing tools for cell therapy work

    The California biotech will receive $25 million upfront from Sanofi, which plans to use Scribe’s platform to edit natural killer cells for cancer treatment.

    By Ned Pagliarulo • Sept. 27, 2022
  • A group of researchers and patients from a research lab at UC San Francisco pose with a large check.
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    Permission granted by Ethan Perlstein and Klein Lab at UCSF
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    Q&A

    Perlara CEO Ethan Perlstein on reviving a biotech and building a ‘Y Combinator of rare diseases’

    The CEO resuscitated the sector’s first public benefit corporation during the pandemic, building an unusually transparent model for biotechs. Now, he’s spun out a startup and is planning for more.

    By Sept. 27, 2022
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    Permission granted by Prime Medicine
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    Prime Medicine becomes the next high-profile biotech to test IPO waters

    The startup, which launched last year with $315 million in funding and plans to advance a new form of gene editing, is one of the first big venture-backed biotechs in several months to seek an IPO.

    By Sept. 26, 2022
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    AstraZeneca gives up on Ionis’ RNA drug for heart disease

    The British drugmaker decided the medicine, which works similarly to Novartis’s Leqvio, wasn’t potent enough to justify further testing. 

    By Sept. 23, 2022
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    Elizabeth Regan/BioPharma Dive
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    Servier cuts ties with Allogene, ending complex CAR-T partnership

    The French drugmaker terminated a nearly decade-old deal that helped Allogene emerge as the sector's largest "off-the-shelf" cell therapy developer.

    By Sept. 22, 2022
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    Getty Images
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    GSK buys into Spero’s comeback plan

    The British drugmaker is investing in Spero Therapeutics and acquiring most of the rights to an oral antibiotic the FDA previously rejected, but could approve if it succeeds in a new Phase 3 trial.

    By Sept. 22, 2022
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    Getty Images
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    Cell therapy startup Carisma merges with troubled Sesen in bid for Wall Street

    The deal results from a strategic review Sesen, formerly known as Eleven Biotherapeutics, undertook after the FDA rejected its top drug last year. 

    By Sept. 21, 2022
  • A photograph of Jan W. Thomsen and Peter Krogstrup Jeppesen, from the University of Copenhagen.
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    Courtesy of University of Copenhagen
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    Foundation behind Novo Nordisk to invest $200M in building quantum research ‘powerhouse’

    The grant is one of the Novo Nordisk Foundation’s largest and will fund a 12-year research collaboration to construct a quantum computer dedicated to the life sciences.

    By Ned Pagliarulo • Sept. 21, 2022
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    Vesalius Therapeutics, a buzzy, Flagship-backed startup, cuts jobs six months after public launch

    When the company debuted in March, it announced plans to hire 200 employees over two years. Now, it’s laid off nearly half its staff in a year when the biotech sector has experienced a sharp market downturn.

    By Sept. 19, 2022
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    Theravance, flush with royalty cash, buys shares from GSK

    The planned transaction will further unwind the respiratory disease company’s relationship with GSK, which dates back two decades.

    By Sept. 19, 2022
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    Getty Images
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    Alnylam, Regeneron to advance NASH drug after early signs of potential

    A gene discovery four years ago led to a partnership between the companies, which plan to start a Phase 2 study later this year after encouraging early data. 

    By Ned Pagliarulo • Sept. 15, 2022
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    Nasdaq
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    Third Harmonic boosts biotech with sector’s top IPO in four months

    The startup’s $185 million initial public offering is the largest for the sector since early May and potentially a sign of renewed investor interest in young biotechs.

    By Sept. 15, 2022
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    Peddalanka Ramesh Babu via Getty Images
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    Pharmas back a startup’s plan to make CAR-T cells inside the body

    Capstan Therapeutics was formed by pioneering CAR-T and messenger RNA researchers and has secured funding from five large drugmakers.

    By Sept. 14, 2022
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    Getty Images
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    MD Anderson launches new spinout to develop radiopharmaceuticals

    The joint venture with Radiopharm Theranostics is pursuing a field of research that’s seen a string of recent deals and investments by large drugmakers. 

    By Kristin Jensen • Sept. 14, 2022
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    Acelyrin sets hopes high for arthritis drug with $300M fundraise

    The well-funded startup is planning Phase 3 trials for a drug it claims could be superior to top-selling medicines from Novartis and others.

    By Sept. 14, 2022
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    Rubius, a once high-flying biotech startup, lays off much of its staff

    The biotech will reduce staff by 75% and end development of two drugs, the latest setback for a company that was worth nearly $2 billion when it went public in 2018.

    By Sept. 13, 2022
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    Danielle Ternes/BioPharma Dive
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    BioMarin reports cancer case in hemophilia gene therapy trial

    The development comes three weeks after Roctavian was approved in Europe and ahead of a planned regulatory submission in the U.S. Drug regulators have not ordered a trial hold, however.

    By Sept. 13, 2022
  • Third Harmonic CEO Natalie Holles
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    Permission granted by Third Harmonic
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    Can biotech IPOs bounce back? Third Harmonic to test investor appetite with planned offering

    The startup is the first young drugmaker in more than four months to seek an IPO of at least $100 million, a once common occurrence that's become rare following this year's sector-wide correction.

    By Sept. 13, 2022
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    Permission granted by Nimbus Therapeutics
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    Nimbus raises $125M to advance rival to Bristol Myers’ new psoriasis drug

    The money will help fund development of a TYK2 inhibitor that Nimbus CEO Jeb Keiper claims is more selective than Bristol Myers’ Sotyktu.

    By Sept. 12, 2022
  • A photo of Bluebird bio signage in a corporate lobby
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    Permission granted by Bluebird bio
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    Bluebird CFO resigns ahead of gene therapy launch

    Jason Cole, who replaced former CFO Gina Consylman in March, is leaving six months later to “pursue new career opportunities,” the company said.

    By Sept. 12, 2022
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    Permission granted by Stig Albansson / Pretzel Therapeutics
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    Mitochondrial drugs, with a twist: Pretzel Therapeutics launches with $72.5M in funding

    Scientists at Pretzel believe fixing mutated mitochondrial DNA with a mix of small molecule therapies and gene editing could be key to solving a number of hard-to-treat diseases.

    By Sept. 12, 2022