XBIO REPORT

  • WEEKLY BIOTECH STOCK CATALYST REPORTS
  • OPTION SCREENERS
  • November 2, 2023

    Aptose Biosciences | Tuspetinib Clinical Data Selected for Oral Presentation at the 2023 ASH Annual Meeting

    NASDAQ: APTO Aptose Biosciences Inc. announced that clinical data for tuspetinib has been selected for oral presentation at the 65th American Society of Hematology Annual Meeting. The presentation will include safety and efficacy data from Aptose’s ongoing APTIVATE trial of tuspetinib in relapsed/refractory acute myeloid leukemia patients. The presentation will take place on December 9,…

    Clinical Trial, Conferences
    annual-meeting, ash, event, events, kidney-week-2023, meeting, press-releases
  • October 28, 2023

    BIO-TECH STOCK CATALYST REPORT FOR WEEK OF OCTOBER 29 – NOVEMBER 4, 2023

    October 28, 2023 EVENT EVENT DATE SYMBOL PRICE POTENTIAL % (+/-) OPEN INTEREST PRICE Conference 11/02/2023 ARDX 22.5 27,193 $3.49 Conference 11/02/2023 ELDN 44.2 278 $1.59 Conference 11/03/2023 ACET 36.3 90 $1.26 Conference 11/03/2023 AUPH 23.5 11,055 $7.19 FDA Event 11/04/2023 CRBP 94.6 6,911 $5.21 WEEK: 10/29/2023 – 11/04/2023

    Weekly Stock Catalyst Report
  • October 20, 2023

    BIO-TECH STOCK CATALYST REPORT FOR WEEK OF OCTOBER 22-28, 2023

    October 20, 2023 EVENT EVENT DATE SYMBOL PRICE POTENTIAL % (+/-) OPEN INTEREST PRICE FDA Event 10/22/2023 REGN 3.0 600 $808.47 Conference 10/22/2023 RVMD 37.7 33,800 $27.97 Conference 10/23/2023 HARP 52.4 307 $6.88 FDA Event 10/26/2023 CPRX 13.9 2,074 $12.80 WEEK: 10/22/2023 – 10/28/2023

    Weekly Stock Catalyst Report
  • October 2, 2023

    Rocket Pharmaceuticals | Unlocking the Potential: RP-L201 and its FDA Designations – A Breakthrough in Pediatric Medicine

    NASDAQ: RCKT Rocket Pharmaceuticals has achieved significant milestones with their groundbreaking therapy, RP-L201. The FDA has granted several prestigious designations to RP-L201, including Regenerative Medicine Advanced Therapy (RMAT), Rare Pediatric, Fast Track, and Orphan Drug designations. These designations highlight the immense potential of RP-L201 in treating pediatric patients and emphasize the urgent need for innovative…

    Clinical Trial, FDA Acceptance
    fda, neurology, pediatric, pr-newswire, press-releases, priority-review, RMAT
  • September 11, 2023

    Aquestive Therapeutics | FDA Acceptance of Libervant™ for Treatment of Seizure Clusters in Young Patients

    NASDAQ: AQST The FDA has recently accepted the New Drug Application (NDA) for Libervant™ (diazepam) Buccal Film, aiming to tackle the treatment of seizure clusters in children between the ages of two and five. This development provides hope for young patients and their families who have pbeen struggling with the challenges of managing seizure clusters.…

    Clinical Trial, FDA Acceptance
    clinical trials, new drug application, pediatric, pr-newswire, press-releases, seizures
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