Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986368, for the Treatment of Agitation in Participants With Alzheimer's Disease

Abroad (travel likely)RecruitingPHASE2

Conditions

Agitation · Alzheimer Disease

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations
  • Local Institution - 0046, Homewood, Alabama, United States

  • University of Alabama - Huntsville Regional Medical Campus, Huntsville, Alabama, United States

    Contact: Study coordinator (Tiffany Schwasinger-Schmidt) · 256-551-4512
  • Local Institution - 0048, Phoenix, Arizona, United States

  • Local Institution - 0040, Scottsdale, Arizona, United States

  • Local Institution - 0017, Anaheim, California, United States

  • Inland Psychiatric Medical Group., Chino, California, United States

    Contact: Study coordinator (Nandita Puchakayala) · 909-488-9116
  • Kaizen Brain Center, La Jolla, California, United States

    Contact: Study coordinator (MOHAMMED AHMED) · 214-893-0542
  • University of California San Diego - La Jolla, La Jolla, California, United States

    Contact: Study coordinator (Gabriel Leger) · 858-246-1303
  • Shreenath Clinical Service - Lakewood, Lakewood, California, United States

    Contact: Study coordinator (ERIC TATE) · 714-717-6039
  • Accellacare - Sherman Oaks, Sherman Oaks, California, United States

    Contact: Study coordinator (Neeraj Gupta) · 562-548-8500
  • Next Level Clinical Trials, West Covina, California, United States

    Contact: Study coordinator (Austina Cho) · 714-999-6688
  • Local Institution - 0028, West Hills, California, United States

  • University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States

    Contact: Study coordinator (Samantha Holden) · 303-724-2046
  • Local Institution - 0067, Washington D.C., District of Columbia, United States

  • Local Institution - 0053, Washington D.C., District of Columbia, United States

  • Arrow Clinical Trials, Daytona Beach, Florida, United States

    Contact: Study coordinator (David Billmeier) · 386-278-8000
  • ClinCloud, Maitland, Florida, United States

    Contact: Study coordinator (Rosemary Laird) · 717-357-1569
  • Local Institution - 0007, Maitland, Florida, United States

  • Local Institution - 0022, Miami, Florida, United States

  • Local Institution - 0010, Miami, Florida, United States

  • Local Institution - 0001, Tampa, Florida, United States

  • Charter Research - Lady Lake, The Villages, Florida, United States

    Contact: Study coordinator (Jeffrey Norton) · 352-775-1000
  • Local Institution - 0026, Atlanta, Georgia, United States

  • CenExel iResearch, LLC, Decatur, Georgia, United States

    Contact: Study coordinator (Kimball Johnson) · 404-537-1281
  • CenExel iResearch, LLC, Savannah, Georgia, United States

    Contact: Study coordinator (Yael Elfassy) · 912-744-0800
  • Local Institution - 0004, Honolulu, Hawaii, United States

  • Local Institution - 0011, Marrero, Louisiana, United States

  • Local Institution - 0051, South Dartmouth, Massachusetts, United States

  • Boeson Research, Missoula, Montana, United States

    Contact: Study coordinator (Lisa Koehl) · 406-543-9700
  • Be Well Clinical Studies - Omaha, Omaha, Nebraska, United States

    Contact: Study coordinator (John Puente) · 402-937-9293
  • Local Institution - 0041, Las Vegas, Nevada, United States

  • Local Institution - 0059, Livingston, New Jersey, United States

  • University at Buffalo - UBMD Neurology, Buffalo, New York, United States

    Contact: Study coordinator (Kinga Szigeti) · 281-630-2316
  • The Feinstein Institute for Medical Research, Manhasset, New York, United States

    Contact: Study coordinator (Jeremy Koppel) · 516-562-3492
  • Mid Hudson Medical Research, New Windsor, New York, United States

    Contact: Study coordinator (Sashi Makam) · 845-674-9398
  • Local Institution - 0064, Staten Island, New York, United States

  • Research Central LLC (DBA Ichor Research), Syracuse, New York, United States

    Contact: Study coordinator (Karl Hafner) · 315-529-0766
  • New Hope Clinical Research, Charlotte, North Carolina, United States

    Contact: Study coordinator (Kurian Abraham) · 980-209-9784
  • UNC Health REX Hospital, Raleigh, North Carolina, United States

    Contact: Study coordinator (Sandeep Vaishnavi) · 919-784-1198
  • Cleveland Clinic, Cleveland, Ohio, United States

    Contact: Study coordinator (Kasia Rothenberg) · 216-403-6847
  • Thomas Jefferson University - Vickie & Jack Farber Institute for Neuroscience, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (James Ellison) · 215-503-2823
  • K2 Medical Research - East Providence, East Providence, Rhode Island, United States

    Contact: Study coordinator (john stoukides) · 401-435-8950
  • Local Institution - 0031, Chattanooga, Tennessee, United States

  • Neurology Clinic, P.C., Cordova, Tennessee, United States

    Contact: Study coordinator (Thomas Arnold) · 901-866-9252
  • Vanderbilt University Medical Center- Village, Nashville, Tennessee, United States

    Contact: Study coordinator (Joshua Smith) · 601-594-0792
  • Pinnacle Clinical Research, Austin, Texas, United States

    Contact: Study coordinator (Rohit Puskoor) · 817-602-5188
  • Horizon Clinical Research Center - Houston, Cypress, Texas, United States

    Contact: Study coordinator (Harpaul Gill) · 949-491-0710
  • ANESC Research, El Paso, Texas, United States

    Contact: Study coordinator (Aamr Herekar) · 505-903-1715
  • North Pointe Psychiatry - Flower Mound, Flower Mound, Texas, United States

    Contact: Study coordinator (Asad Islam) · 469-444-2244
  • Local Institution - 0020, Houston, Texas, United States

  • Stryde Research - Plano, Plano, Texas, United States

    Contact: Study coordinator (Peter Brokish) · 214-407-8640
  • Be Well Clinical Studies, Round Rock, Texas, United States

    Contact: Study coordinator (Mark Carlson) · 000-000-0000
  • Boeson Research - Provo, Provo, Utah, United States

    Contact: Study coordinator (Jason Andersen) · 385-392-2200
Study leads
  • Bristol-Myers Squibb

    Study Director

    Bristol-Myers Squibb