Public Health Emergency: SOLIDARITY TRIAL Philippines
NCT05024006 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1314
Last updated 2022-03-02
Summary
This study is an adaptive, randomized, open-label, controlled clinical trial utilizing an adaptive design to compare effects of repurposed drugs with local standard of care alone on major inpatient hospital outcomes. This is performed worldwide in collaboration with WHO.
Conditions
- Covid19
Interventions
- DRUG
-
Remdesivir
Two intravenous loading doses, then daily infusion for 10 days
- DRUG
-
Hydroxychloroquine
Two oral loading doses, then orally twice daily for 10 days
- DRUG
-
Lopinavir / Ritonavir
Orally twice daily for 14 days
- DRUG
-
Interferon beta-1a
Daily injection for 6 days
- DRUG
-
Orally twice daily for 10 days
Sponsors & Collaborators
-
University of the Philippines
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-04-23
- Primary Completion
- 2021-04-17
- Completion
- 2021-04-17
Countries
- Philippines
Study Locations
More Related Trials
-
Pilot Study: Oral Treatment of American Tegumentary Leishmaniasis (Cutaneous and Mucosal Forms) in the Elderly
NCT06040489 ·Status: RECRUITING ·Phase: PHASE2/PHASE3
-
A Study to Determine Safety, Tolerability, and Pharmacokinetics of Different Orally Administered Regimens of the Combination ZY19489-Ferroquine in Adult Asymptomatic Plasmodium Falciparum Carriers
NCT05911828 ·Status: RECRUITING ·Phase: PHASE1
-
Platform Study to Evaluate the Efficacy and Safety of Anti-malarial Agents in Participants With Uncomplicated Plasmodium Falciparum Malaria (Cohort B2)
NCT07235033 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy, Safety, Tolerability and Pharmacokinetics of KAE609 in Adult Patients With Acute, Uncomplicated Plasmodium Falciparum or Vivax Malaria Mono-infection
NCT01524341 ·Status: COMPLETED ·Phase: PHASE2
-
A Clinical Trial to Evaluate the Efficacy of RUTI® to Reduce the Severity of SARS-CoV-2 Infection (COVID-19)
NCT05115019 ·Status: WITHDRAWN ·Phase: PHASE2/PHASE3
-
Combination Assessment Trial of COVID-19 Vaccines (COMBAT-COVID)
NCT05162482 ·Status: UNKNOWN ·Phase: PHASE2
-
Malaria Challenge in Healthy Volunteers
NCT01500980 ·Status: COMPLETED ·Phase: PHASE1
-
Controlled Human Malarial Infection by Intravenous Injection of Plasmodium Falciparum Sporozoites in Non-Immune Adults
NCT01624961 ·Status: COMPLETED ·Phase: PHASE1
-
Exploratory Study to Evaluate the Efficacy of RUTI® Against SARS-COV-2 Infection (COVID-19) in Healthcare Workers
NCT04903184 ·Status: COMPLETED ·Phase: PHASE2
-
Immunization With Different Doses of Plasmodium Falciparum Sporozoites Under Chloroquine Prophylaxis
NCT01218893 ·Status: COMPLETED ·Phase: NA
-
A Study Of Zy-19489 Administered Via Oral Route To Investigate The Safety, Tolerability And Pharmacokinetics In Healthy Adult Human Subjects
NCT05206201 ·Status: COMPLETED ·Phase: PHASE1
-
21-day Double-blind Trial of Albendazole in Adults With Loa Loa Microfilaremia
NCT06613997 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Efficacy, Safety, Tolerability and Pharmacokinetics of KAF156 in Adult Patients With Acute, Uncomplicated Plasmodium Falciparum or Vivax Malaria Mono-infection
NCT01753323 ·Status: COMPLETED ·Phase: PHASE2
-
Clinical Trial to Assess the Safety and Efficacy of Sodium Stibogluconate (SSG) and AmBisome® Combination, Miltefosine and AmBisome® and Miltefosine Alone for the Treatment Visceral Leishmaniasis in Eastern Africa
NCT01067443 ·Status: COMPLETED ·Phase: PHASE2
-
Comparison of Three Plasmodium Falciparum Isolates in an Experimental Human Malaria Infection
NCT01002833 ·Status: COMPLETED ·Phase: NA
-
Open-Label, Sequential Step, Safety and Efficacy Study to Determine the Optimal Single Dose of Ambisome for Patients With VL
NCT00832208 ·Status: TERMINATED ·Phase: PHASE2
-
Amphotericin B to Treat Visceral Leishmaniasis in Brazilian Children
NCT01032187 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy of SJ733 in Adults With Uncomplicated Plasmodium Falciparum or Vivax Malaria
NCT04709692 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Assess the Experimental Malaria Vaccines RH5.2-VLP and R21
NCT05357560 ·Status: COMPLETED ·Phase: PHASE1
-
Adjunctive Ivermectin Mass Drug Administration for Malaria Control
NCT04844905 ·Status: UNKNOWN ·Phase: PHASE3
-
Anti-malaria MAb in Malian Children
NCT05304611 ·Status: COMPLETED ·Phase: PHASE2
-
A Clinical Trial to Evaluate the Safety, Efficacy and Immune Responses After Vaccination With an Investigational RNA-based Vaccine Against Malaria
NCT06069544 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Effect of Combined Use of Ivermectin and Colchicine in COVID-19 Patients
NCT05246072 ·Status: COMPLETED ·Phase: PHASE4
-
International Registry of Healthcare Workers Exposed to COVID-19 Patients (UNITY Global)
NCT04626076 ·Status: COMPLETED
-
Immuno-bridging Study of COVID-19 Protein Subunit Recombinant Vaccine
NCT05433285 ·Status: COMPLETED ·Phase: PHASE3