Bipolar Disorder with Depression Treatment

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY FOLLOWED BY OPEN-LABEL TREATMENT OF ALTO-100 IN ADULTS WITH BIPOLAR DISORDER CURRENTLY EXPERIENCING A MAJOR DEPRESSIVE EPISODE

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Major Depressive Disorder with Insomnia Symptoms

Double-Blind, Randomized Placebo-Controlled Study to Evaluate Efficacy and Safety and the Maintenance of Effect of 20-mg Seltorexant as Adjunctive Therapy to Antidepressants in Adult and Elderly Patients with Major Depressive Disorder with Insomnia Symptoms

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Participants with Type 2 Diabetes and Obesity

Investigational Tirzepatide Doses in Participants with Type 2 Diabetes and Obesity

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Upcoming Studies for Men & Women

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ADEPT-4 Alzheimer's Disease Psychosis Treatment

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of KarXTfor the Treatment of Psychosis Associated with Alzheimer’s Disease (ADEPT –4 )

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Prevention of Gluten-Specific T Cell Activation in Subjects with Celiac Dis

The ILLUMINATE-101 clinical research study is evaluating the safety and effectiveness of an investigational medication designed to reduce or eliminate the negative immune response to gluten in adults with celiac disease and participants are needed.

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Uterine Fibroids or Moderate to Severe Pain Associated with Endometriosis

Open-Label Study to Evaluate Bone Mineral Density with Long-Term Use of Relugolix Combination Tablet in Premenopausal Women with Heavy Menstrual Bleeding Associated with Uterine Fibroids or Moderate to Severe Pain Associated with Endometriosis

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RSV Ag Rapid Test Cassette in Detecting RSV Infection in any Age group

Study to Evaluate the Performance and Feasibility of AssureTech RSV Ag Rapid Test Cassette in Detecting RSV Infection in any Age group

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A Study to Evaluate the Safety and Efficacy of Flu Vaccine for Prevention o

A Novel Long-Acting Antiviral Conjugate, for the Prevention of Influenza in Adults and Adolescents at Higher Risk of Developing Influenza Complications

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Airsupra Asthma Study

A Randomized, Placebo-controlled, Double-blind, Multicenter, 12‑Week, 3-Way, Partial-replicate Crossover Pharmacodynamic Study to Assess the Equivalence of Budesonide and Albuterol (BDA) Delivered by MDI HFO Compared with BDA Delivered by MDI HFA in Participants with Asthma

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