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Clinical trials

  • CorEvitas-IBD-600

    This prospective, non-interventional research registry is designed to study the comparative effectiveness and comparative safety of approved treatments for IBD in a cohort of patients cared for by gastroenterologists across North America. Secondary鈥�

    Investigator
    Angela Pham
    Ages
    18 Years - N/A
    Sexes
    All
  • M23-784

    Crohn's disease (CD) is a long-lasting disease that causes severe inflammation (redness, swelling), in the digestive tract, most often affecting the bowels. It can cause many different symptoms including abdominal pain, diarrhea, tiredness, and鈥�

    Investigator
    Angela Pham
    Ages
    18 Years - N/A
    Sexes
    All
  • AbbVie M23-703

    Ulcerative colitis (UC) is a type of inflammatory bowel disease that causes inflammation and bleeding from the lining of the rectum and colon (large intestine). The purpose of this study is to assess how safe and effective lutikizumab is in adult鈥�

    Investigator
    Angela Pham
    Ages
    18 Years - N/A
    Sexes
    All
  • Palekona-GS-US-457-6411

    The goal of this study is to learn if tilpisertib fosmecarbil (formerly known as GS-5290) is effective and safe in treating participants with moderate to severe ulcerative colitis. The study will compare participants in different treatment groups鈥�

    Investigator
    Angela Pham
    Ages
    18 Years - 75 Years
    Sexes
    All
  • Rhythm_RM-493-035

    The protocol describes a randomized, double-blind, placebo-controlled trial with independent sub-studies of setmelanotide in patients with obesity and at least one of the specific gene variants in the Melanocortin-4 Receptor pathway: POMC or PCSK1鈥�

    Investigator
    Angelina V Bernier
    Ages
    6 Years - 65 Years
    Sexes
    All
  • MK-7240

    The purpose of this protocol is to evaluate the efficacy of tulisokibart in participants with moderately to severely active ulcerative colitis. Study 1's primary hypotheses are that at least 1 tulisokibart dose level is superior to Placebo in the鈥�

    Investigator
    Angela Pham
    Ages
    16 Years - 80 Years
    Sexes
    All
  • MOM-M281-006

    The main purpose of this study is to evaluate the efficacy and safety of M281 in participants with warm autoimmune hemolytic anemia (wAIHA).

    Investigator
    Anita Rajasekhar
    Ages
    18 Years - N/A
    Sexes
    All
  • FASTEST Trial

    The objective of the rFVIIa for Acute Hemorrhagic Stroke Administered at Earliest Time (FASTEST) Trial is to establish the first treatment for acute spontaneous intracerebral hemorrhage (ICH) within a time window and subgroup of patients that is鈥�

    Investigator
    Anna Y Khanna
    Ages
    18 Years - 80 Years
    Sexes
    All
  • Saturn

    The SATURN trial aims to determine whether continuation vs. discontinuation of statin drugs after spontaneous lobar intracerebral hemorrhage (ICH) is the best strategy; and whether the decision to continue/discontinue statins should be influenced by鈥�

    Investigator
    Anna Y Khanna
    Ages
    50 Years - N/A
    Sexes
    All