Oral Ifetroban in Patients With Idiopathic Pulmonary Fibrosis (IPF)

Abroad (travel likely)RecruitingPHASE2

Conditions

Idiopathic Pulmonary Fibrosis

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
  • Biosolutions Clinical Research, La Mesa, California, United States

    Contact: Principal Investigator (Kaveh Bagheri, MD)
  • University of California San Francisco, San Francisco, California, United States

    Contact: Study coordinator (Asha Payda) · ashapayda2@ucsf.edu · 415-476-7054
    Contact: Principal Investigator (Jeffrey Golden, MD)
  • Mayo Clinic Jacksonville, Jacksonville, Florida, United States

    Contact: Study coordinator (Jennifer Singh) · singh.jennifer@mayo.edu · 904-953-3855
    Contact: Principal Investigator (Augustine Lee, MD)
  • Miami VA Health System, Miami, Florida, United States

    Contact: Study coordinator (Carol Ramos) · carol.ramos@va.gov · 305-310-2614
    Contact: Principal Investigator (Robert Jackson, MD)
  • Northwestern Medicine, Chicago, Illinois, United States

    Contact: Study coordinator (Bailey Damore) · bailey.damore@northwestern.edu · 312-503-5242
    Contact: Principal Investigator (Krishnan Warrior, MD)
  • Indiana University Health, Indianapolis, Indiana, United States

    Contact: Study coordinator (Kim McPeak) · kmcpeak@iuhealth.org · 317-962-1138
    Contact: Principal Investigator (Damien Patel, MD)
  • University of Kansas, Kansas City, Kansas, United States

    Contact: Study coordinator (Chelsea Aulukh) · ckirtley@kumc.edu · 913-588-2812
    Contact: Principal Investigator (Mark Hamblin, MD)
  • University of Louisville, Louisville, Kentucky, United States

    Contact: Study coordinator (Belica Graf) · belica.graf@louisville.edu · 502-852-0560
    Contact: Principal Investigator (Mohamed Saad, MD)
  • Beaumont Hospital, Royal Oak, Royal Oak, Michigan, United States

    Contact: Study coordinator (Coleen Tessmar) · coleen.tessmar@beaumont.org · 248-551-0312
    Contact: Principal Investigator (Enrique Calvo-Ayala, MD)
  • Icahn School of Medicine at Mount Sinai, New York, New York, United States

    Contact: Study coordinator (Olia Ali) · olia.ali@mssm.edu · 347-393-6217
    Contact: Principal Investigator (Maria Padilla, MD)
  • University of Rochester, Rochester, New York, United States

    Contact: Study coordinator (Karen McCarthy) · karen_mccarthy@urmc.rochester.edu · 585-276-7294
    Contact: Principal Investigator (David Nagel, MD, PhD)
  • UNC Chapel Hill, Chapel Hill, North Carolina, United States

    Contact: Study coordinator (Jackson Pettee) · jackson.pettee@med.unc.edu · 919-843-4450
  • Bend Memorial Hospital, Bend, Oregon, United States

    Contact: Study coordinator (Natanya Hernandez) · nahernandez@summithealth.com · 541-706-2302
    Contact: Principal Investigator (Jeremy Feldman, MD)
  • Temple University Hospital, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (John Valkovec) · john.valkovec@tuhs.temple.edu · 2157076028
    Contact: Principal Investigator (Gerard Criner, MD)
  • Avera Research Institute, Sioux Falls, South Dakota, United States

    Contact: Study coordinator (Shelby Petereit) · shelby.petereit@avera.org · 605-504-3151
    Contact: Principal Investigator (Fady Jamous, MD)
  • Pulmonary & Sleep Specialists, Dickson, Tennessee, United States

    Contact: Study coordinator (Chloe Alberd) · chloealberd@gmail.com · 615-375-1531
    Contact: Principal Investigator (Mohammad Alsoub, MD)
  • Baylor University Medical Center, Dallas, Texas, United States

    Contact: Study coordinator (Brianna Kamran) · Brianna.Kamran@BSWHealth.org · (214) 820-1685
    Contact: Principal Investigator (Susan Mathai, MD)
  • Premier Pulmonary Critical Care and Sleep Medicine, Denison, Texas, United States

    Contact: Study coordinator (Muhammad (Mo) Butt) · crc@premierpsm.com · 469-714-9864
    Contact: Principal Investigator (Sanober Kable, MD)
  • UW Health University Hospital, Madison, Wisconsin, United States

    Contact: Study coordinator (Yuliya Henes) · yhenes@clinicaltrials.wisc.edu · 608-262-1789
Study leads
  • Todd Rice, MD, MSc

    Principal Investigator

    Cumberland Pharmaceuticals