CPX101-Ⅱ-01 Obese Subjects without Diabetes Mellitus

A Randomized, Double-blind, Placebo-controlled, Parallel-group Multicenter Trial to Evaluate the Safety and Efficacy of CPX101 in Overweight and Obese Subjects without Diabetes Mellitus

CONDITION: Metabolic and Endocrine

GENDER: All

AGE GROUP: 18 to 75 years

TRIAL STATUS: Active, not recruiting

CIC-E-301

A Phase 3, Randomized, Observer-Blinded, Active-Controlled Study to Evaluate the Safety and Immunogenicity of a SARS‑CoV‑2 rS Nanoparticle and Trivalent Hemagglutinin Nanoparticle Influenza Combination Vaccine with Matrix-M™ Adjuvant and a …

CONDITION: Other

GENDER: All

AGE GROUP: 60 and above

TRIAL STATUS: Active, not recruiting

GS-US-563-5925: People With HIV-1 Who Are Virologically Suppressed on Bictegravir/Emtricitabine/Tenofovir

A Phase 3, Randomized, Active-controlled, Double-blind Study to Evaluate a Switch to an Oral Weekly Islatravir/Lenacapavir Regimen in People With HIV-1 Who Are Virologically Suppressed on Bictegravir/Emtricitabine/Tenofovir (B/F/TAF)

CONDITION: Other

GENDER: All

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

GS-US-563-5926: Oral Weekly Islatravir/ Lenacapavir Regimen in People with HIV-1 Who are Virologically Suppressed on Standard of Care

A Phase 3 Randomized, Active-Controlled, Open-Label Study to Evaluate a Switch to an Oral Weekly Islatravir/ Lenacapavir Regimen in People with HIV-1 Who are Virologically Suppressed on Standard of Care

CONDITION: Other

GENDER: All

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

I7P-MC-DSAF: Moderate to Severe Hidradenitis Suppurativa

A Phase 2b, Double-Blind, Placebo-Controlled Study to Evaluate Eltrekibart in Adult Participants with Moderate to Severe Hidradenitis Suppurativa

CONDITION: Skin

GENDER: All

AGE GROUP: 18 to 75 years

TRIAL STATUS: Active, not recruiting

GS-US-536-5939: Virologically Suppressed Adults With HIV-1 Infection

A Phase 2 Randomized, Open-label Study to Evaluate the Safety and Efficacy of Broadly Neutralizing Antibodies (bNAbs) GS-5423 and GS-2872 in Combination With the Capsid Inhibitor Lenacapavir as Long-Acting Treatment …

CONDITION: Other

GENDER: All

AGE GROUP: 18 to 65 years

TRIAL STATUS: Active, not recruiting

A Phase IIIb, Randomized, Multicenter, Parallel-group, Non-inferiority, Open-label Study Evaluating the Efficacy, Safety, and Tolerability of Long-acting Cabotegravir Plus Long-acting Rilpivirine Administered Every 8 Weeks or Every 4 Weeks in HIV-1-infected Adults Who Are Virologically Suppressed

This Antiretroviral Therapy as Long Acting Suppression every 2 Months (ATLAS-2M) study is designed to demonstrate the non-inferior antiviral activity and safety of CAB LA + RPV LA administered every …

CONDITION: Inflammatory and Immune System

GENDER: All

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

Study to Compare Bictegravir/Lenacapavir Versus Current Therapy in People With HIV-1 Who Are Successfully Treated With Biktarvy (ARTISTRY-2)

This study is being done to see how well a new HIV treatment works compared to current standard treatment. Researchers are testing a single tablet that combines bictegravir (BIC) and …

CONDITION: Inflammatory and Immune System

GENDER: All

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

Phase 3 Trial of Bictegravir/Lenacapavir Fixed-Dose Combination (single daily pill) vs Standard HIV Therapy – ARTISTRY 1

This study is for people living with HIV whose treatment is already keeping the virus under control. Researchers are testing whether switching to new medicines, bictegravir and lenacapavir (together in …

CONDITION: Inflammatory and Immune System

GENDER: All

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

A Phase 3 Study Evaluating the Safety and Effectiveness of Switching to a Once-Weekly Islatravir/Lenacapavir Regimen Compared to Continuing Standard Daily HIV Therapy in Virologically Suppressed Adults – ISLEND 2

This study is testing whether people with HIV whose virus is already well controlled can safely switch from their current daily HIV medicines to a new once-a-week pill (islatravir/lenacapavir).

CONDITION: Inflammatory and Immune System

GENDER: All

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

A Phase 3 Study of Switching from Daily to Weekly Oral HIV Treatment – ISLEND 1

This is a large final-stage (Phase 3) clinical trial testing whether people living with HIV, who already have their virus under control on the standard daily HIV pill (Biktarvy® – …

CONDITION: Inflammatory and Immune System

GENDER: Both males and females

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

Do you have non-alcoholic steatohepatitis (NASH)?

Australian researchers are testing a new treatment for non-alcoholic steatohepatitis (NASH), an advanced form of non-alcoholic fatty liver disease (NAFLD). A new medication is to be taken orally 3 times …

CONDITION: Inflammatory and Immune System

GENDER: Both males and females

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

Clinical trial of Sailuotong (SLT) for Vascular Dementia or Alzheimer’s Disease with evidence of cerebrovascular disease

SLT for Vascular Dementia Vascular dementia (VaD) is the second major cause of dementia accounting for 15-20 per cent of all dementia cases. VaD is an acquired cognitive impairment due …

CONDITION: Neurological

GENDER: Both males and females

AGE GROUP: 40 and above

TRIAL STATUS: Active, not recruiting

Adolescent Atopic Dermatitis Trial (72 Weeks)

Youth aged 12 to 17 with a history of eczema (atopic dermatitis) for at least one year, may qualify to participate in this study. Adolescents must have moderate to severe …

CONDITION: Skin

GENDER: Both males and females

AGE GROUP: 12 to 17 years

TRIAL STATUS: Active, not recruiting

RESTORE Clinical Trial for Back Pain – Perth

The RESTORE clinical trial is a large scale research study in Australia exploring back pain treatments. We are trying to measure how effective existing treatments are for people with persistent …

CONDITION: Musculoskeletal

GENDER: Both males and females

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting

CAIN457A3404 (REALIA)

Title: A non-interventional, prospective 12 months study to characterize the REAL-life effectiveness and treatment patterns of Secukinumab and current standard of care in patient with chronic plaque psoriAsis eligible for …

CONDITION: Skin

GENDER: Both males and females

AGE GROUP: 18 and above

TRIAL STATUS: Active, not recruiting