17,261 trials
Melanoma
Primary: Dose Limiting Toxicity (DLT) [Phase I] — 1 Participants
Alzheimer Disease
Primary: Cytochrome Oxidase/Citrate Synthase (COX/CS) Activity — -0.0000049; 0.0000195; 0.0000245 1/(seconds multiplied by micromoles) — p=>0.05
NASH - Nonalcoholic Steatohepatitis
Primary: Safety and Tolerability of LPCN 1144 — 10 Participants
Leukemia, Lymphoid · Lymphoma, Non-Hodgkin · Lymphoma, Mantle-Cell
Primary: Primary Analysis Set (PAS): Overall Response Rate (ORR) Assessed by Independent Review Committee — 71.4 Percentage of participants
T-Cell Lymphoma Relapsed · T-Cell Lymphoma Refractory
Primary: Best Overall Response Rate During the First 8 Cycles of Treatment — 5 Participants
Acute Myeloid Leukemia (AML) · Myelodysplastic Syndrome (MDS) · Hematopoietic Stem Cell Transplant (HSCT)
Primary: Number of Non-relapsed Deaths by 100 Days Post-transplant in Pediatric Patients Receiving a Myeloablative or Reduced-intensity Preparative Regimen Prior to HSCT for…
Sickle Cell Disease · Vaso-occlusive Crisis
Primary: Pain Score — 5.7 score on a scale
Prader-Willi Syndrome · Obesity
Primary: Microbiome Analysis: Alpha Diversity — 4.89 Shannon index
Cigarette Smoking · Nicotine Dependence
Primary: 7-Day Point Prevalence Abstinence — 30; 44 Participants
Multiple Myeloma
Primary: Overall Response Rate (ORR) — 62.2; 65.1; 50.6 percentage of participants
Resting Energy Expenditure · Thermogenesis · Brown Adipose Tissue
Primary: Cumulative Resting Energy Expenditure — 456.4; 494.7; 481.3; 492.8 kcal
Colitis, Ulcerative
Primary: Percentage of Participants in Clinical Response at Week 12 — 53.8; 50.0 Percentage of participants
Status Epilepticus, Electrographic · Coma
Primary: Primary Pharmacologic Outcome - Absorption — 6; 0 Participants
Infections, Respiratory · Virus Diseases · Infection Viral
Primary: Number of Participants With Solicited Local Reactions at the Injection Site (Pain, Tenderness, Erythema/Redness, Induration/Swelling) Recorded up to 7 Days After Each…
Hepatitis C Infection · HIV Infection
Primary: Percentage of Participants With Sustained Virologic Response at 12 Weeks Post Treatment Discontinuation (SVR12) — 84.4 percentage of participants