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Found 1243 All Conditions trials

A listing of All Conditions medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

 To identify reliable markers of LRRK2 activity in human CSF.
30 years - 99 years
Accepts healthy volunteer
All genders
The purpose of this research study is to evaluate new tests for Parkinson's disease (PD) that may help in developing better treatments.
 Edwards EVOQUE Transcatheter Tricuspid Valve Replacement: Pivotal Clinical Investigation of Safety and Clinical Efficacy using a Novel Device
18 years - 99 years
All genders
Interventional
The research study is being conducted to determine the safety and effectiveness of an investigational device, called the Edwards EVOQUE Replacement system (EVOQUE system) with Optimal Medical Therapy (OMT) compared to OMT alone for the treatment of tricuspid valve regurgitation (TR)
 STRIDE Study : The Effects of semaglutide on functional capacity in pith type 2 diabetes and peripheral arterial disease
18 years - 99 years
All genders
Phase 3
This is a 52 week, randomized, double-blind, placebo-controlled trial comparing semaglutide 1 mg versus placebo both added to standard of care and administered once weekly in subjects with Type 2 Diabetes Mellitus with Intermittent Claudication.
 A071701 Genomically-Guided Treatment Trial in Brain Metastases
18 years - 99 years
All genders
Interventional
This phase II trial studies how well genetic testing works in guiding treatment for patients with solid tumors that have spread to the brain. Several genes have been found to be altered or mutated in brain metastases such as NTRK, ROS1, CDK or PI3K. Medications that target these genes such …
 A Randomized Study to Compare Efficacy  Safety  and Tolerability of Macitentan 75mg Versus Macitentan 10mg in Patients with Pulmonary Arterial Hypertension  Followed by an Open-label Treatment Period with Macitentan 75mg
18 years - 75 years
All genders
Phase 3
TThe research study is being conducted to compare macitentan 75 mg with the approved macitentan 10 mg to see if it is well tolerated, safe and useful for treating patients with pulmonary arterial hypertension (PAH).
 GMCI plus Standard of Care Immune Checkpoint Inhibitor for Stage III/IV NSCLC Patients (LuTK02)
18 years - 99 years
All genders
This trial is to evaluate the safety and efficacy of adding GMCI to standard of care in patients with stage III/IV NSCLC that are not responding to a first line immune checkpoint inhibitor (ICI).
 A Randomized  Double-Blind  Placebo-Controlled  Active Comparator Phase 2/3 Study of Tucatinib in Combination With Trastuzumab  Ramucirumab  and Paclitaxel in Subjects With Previously Treated  Locally-Advanced Unresectable or Metastatic HER2+ Gastric or Gastroesophageal Junction Adenocarcinoma (GEC)
19 years - 99 years
All genders
This study is being done to see if tucatinib with trastuzumab, ramucirumab and paclitaxel works better than ramucirumab and paclitaxel to treat HER2-positive (HER2+) cancer of the gut (stomach or gastroesophageal cancer). This study will also look at what side effects happen when participants take this combination of drugs
 Study of Surufatinib in Combination with Tislelizumab in Subjects With Advanced Solid Tumors
18 years - 99 years
All genders
Phase 1
Interventional
study of surufatinib in combination with tislelizumab will evaluate the safety, and tolerability in patients with advanced solid tumors.
 Study Of Avb-S6-500 In Combination With Cabozantinib Versus Cabozantinib Alone In Patients With Advanced Clear Cell Renal Cell Carcinoma Who Have Received Front-Line Treatment
18 years - 99 years
All genders
Phase 2
This is a Phase 1b/2 study of AVB-S6-500 designed to evaluate the safety and efficacy of AVB-S6-500 in combination with cabozantinib in subjects with advanced clear cell renal cell carcinoma (ccRCC) that have received front-line treatment.
 Apneic Oxygenation to Prevent Oxygen Desaturation During Intubation in the NICU: A Randomized Trial
99 years or below
All genders
The objective of this study is to determine whether apneic oxygenation (nasal cannula 6L/min with FiO2 100%) delivered during laryngoscopy and tracheal intubation, compared with no respiratory support or oxygenation during laryngoscopy and tracheal intubation attempts (standard of care), reduces the magnitude of oxygen desaturation during tracheal intubation encounters in …
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