Articles

  • 5 days ago | thereader.com | Ryan Syrek

    The “point” of Sinners, a rip-snorting vampire-centric music video, is not that “human beings are the real monsters.” The point of Sinners is a stake, driven through the heart of monsters of all-kinds, fanged or not. It is also that the most important thing in life is having a good time with the ones you love and also not summoning unholy hell-beasts by playing music that is simply too good. You are safest playing bad music.

  • 1 week ago | thereader.com | Ryan Syrek

    In the last week, I saw the movie Warfare, and I learned that someone who used to write here in the film section at The Reader died. Maddeningly, painfully, for the second time in less than a year, I find myself crafting something that is closer to a eulogy than it is a movie review. At least this one isn’t my hot take on an animated family film?

  • 2 weeks ago | oncologynewscentral.com | Ryan Syrek |Youssef Rddad

    The U.S. Food and Drug Administration (FDA) granted full approval to larotrectinib (Vitrakvi) for adults and children with NTRK fusion–positive solid tumors that are metastatic, unresectable, or have no other treatment options, drugmaker Bayer announced in an April 10 news release. Regulators based the latest decision on pooled data from the three single-group studies. These included results from the phase 1 LOXO-TRK-14001 trial, the phase 1/2 SCOUT trial, and the phase 2 NAVIGATE trial.

  • 2 weeks ago | thereader.com | Ryan Syrek

    Casting Michael Fassbender as a militant wife guy who hates liars is certainly a choice when the Wikipedia on his personal life is just right there. Ew.If it helps you endure that knowledge, Black Bag isn’t a sweet love song to marriage so much as a synth-jazz tune about loyalty.

  • 2 weeks ago | patientpower.info | Ryan Syrek

    On March 28, 2025, the U.S. Food and Drug Administration approved neoadjuvant durvalumab (Imfinzi) plus gemcitabine and cisplatin, followed by single-agent adjuvant durvalumab after radical cystectomy, for adults with muscle-invasive bladder cancer (MIBC). The FDA based the approval on results from the randomized, open-label, multicenter, phase 3 NIAGARA trial. The study enrolled 1,063 patients with MIBC who had not received prior systemic therapy and were eligible for radical cystectomy.

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