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Clinical Trials Search Results

Multi-dose, Placebo-controlled Study to Evaluate the Efficacy, Safety and Tolerability of treatment of Pruritus in Patients With Primary Biliary Cholangitis (PBC)

Principal Investigator:Stuart C Gordon, MD

Status: Open

Contact Phone: (313) 916-8423

Contact Email: GIHepatotogyClinicalTrials@hfhs.org

PCYC-1128-CA: A Phase 1b/2 Study of Ibrutinib Combination Therapy in Selected Advanced Gastrointestinal And Genitourinary Tumors

Principal Investigator:Ding Wang, MD

Status: Accepting Participants

Contact Phone: (313) 916-7453

Contact Email: CTOResearch@hfhs.org

A 12 months, open-label, multicenter, randomized, safety. efficacy, pharmacokinetic (PK) and pharmacodynamic (PD) study of two regimens of an anti-CD40monoclonal antibody, CFZ533 vs. standard of care control, in adult de novo Liver transplant recipients with a 12 -month additional follow-up

Principal Investigator:Nadeen Khoury, MD

Status: Open

Contact Phone: (313) 916-4596

Contact Email: transplantresearch@hfhs.org

A 12-week, Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Safety and Efficacy of Therapy in Patients With Diabetic Gastroparesis

Principal Investigator:Eva H Alsheik, MD

Status: Open

Contact Phone: (313) 916-8423

Contact Email: GIHepatologyClinicalTrials@hfhs.org

A 14-week, Double-blind, Randomized, Three-arm, Parallel Group Study to Assess the Efficacy and Safety of Two Doses of Pridopidine Versus Placebo for the Treatment of Levodopa-induced Dyskinesia in Patients With Parkinson's Disease (gLIDe)

Principal Investigator:Neepa J Patel, MD

Status: Accepting Participants

Contact Phone: (248)661-6540

Contact Email: parkinsons@hfhs.org

A 3-Part Adaptive Design Study to Assess Safety, Tolerability and Efficacy of Treatment in Patients with Non-alcoholic Steatohepatitis (NASH)

Principal Investigator:Kimberly A Brown, MD

Status: Open

Contact Phone: (313) 916-8423

Contact Email: GIHepatologyClinicalTrials@hfhs.org

A Comparison Study Of Implanted Disolving Investigational Sustained Relased Ocular Medication To Standard Of Care Treatment Procedure For Patients With Open Angle Glaucoma Or Ocular Hypertension

Principal Investigator:David A Crandall, MD

Status: Accepting Participants

Contact Phone: (313) 916-8500

Contact Email: EyeTrials@hfhs.org

A Double-Blind, Placebo-Controlled Proof-of-Concept Study Evaluating Therapy in Patients with Primary Biliary Cholangitis (PBC) Who Have an Inadequate Response or Are Intolerant of UDCA

Principal Investigator:Stuart C Gordon, MD

Status: Open

Contact Phone: 313-916-8423

Contact Email: GIHepatologyClinicalTrials@hfhs.org

A Multi-Center Comparison Study Involving Intravitreal Injections for Central-Involved Diabetic Macular Edema sponsored by Diabetic Retinopathy Clinical Research Network sponsored by the NIH

Principal Investigator:Paul A Edwards, MD

Status: Accepting Participants

Contact Phone: (313) 916-8500

Contact Email: EyeTrials@hfhs.org

A Multi-Center Open-Label Phase 1/2 Study of BGB324 in Combination with Erlotinib in Patients with Stage IIIb or Stage IV Non-Small Cell Lung Cancer (BGBC004)

Principal Investigator:Igor I Rybkin, MD

Status: Accepting Participants

Contact Phone: (313) 916-7453

Contact Email: TOCtrials@hfhs.org

Page 1 of 32 | Results 1 - 10 of 314

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Clinical Trials Search Results

Multi-dose, Placebo-controlled Study to Evaluate the Efficacy, Safety and Tolerability of treatment of Pruritus in Patients With Primary Biliary Cholangitis (PBC)

PCYC-1128-CA: A Phase 1b/2 Study of Ibrutinib Combination Therapy in Selected Advanced Gastrointestinal And Genitourinary Tumors

A 12 months, open-label, multicenter, randomized, safety. efficacy, pharmacokinetic (PK) and pharmacodynamic (PD) study of two regimens of an anti-CD40monoclonal antibody, CFZ533 vs. standard of care control, in adult de novo Liver transplant recipients with a 12 -month additional follow-up

A 12-week, Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Safety and Efficacy of Therapy in Patients With Diabetic Gastroparesis

A 14-week, Double-blind, Randomized, Three-arm, Parallel Group Study to Assess the Efficacy and Safety of Two Doses of Pridopidine Versus Placebo for the Treatment of Levodopa-induced Dyskinesia in Patients With Parkinson's Disease (gLIDe)

A 3-Part Adaptive Design Study to Assess Safety, Tolerability and Efficacy of Treatment in Patients with Non-alcoholic Steatohepatitis (NASH)

A Comparison Study Of Implanted Disolving Investigational Sustained Relased Ocular Medication To Standard Of Care Treatment Procedure For Patients With Open Angle Glaucoma Or Ocular Hypertension

A Double-Blind, Placebo-Controlled Proof-of-Concept Study Evaluating Therapy in Patients with Primary Biliary Cholangitis (PBC) Who Have an Inadequate Response or Are Intolerant of UDCA

A Multi-Center Comparison Study Involving Intravitreal Injections for Central-Involved Diabetic Macular Edema sponsored by Diabetic Retinopathy Clinical Research Network sponsored by the NIH

A Multi-Center Open-Label Phase 1/2 Study of BGB324 in Combination with Erlotinib in Patients with Stage IIIb or Stage IV Non-Small Cell Lung Cancer (BGBC004)