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NCT ID: NCT04389840 Terminated - Acute Lung Injury Clinical Trials

Dociparstat for the Treatment of Severe COVID-19 in Adults at High Risk of Respiratory Failure

Start date: July 8, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

This was a randomized, double-blind, placebo-controlled Phase 2/3 study to evaluate the safety and efficacy of dociparstat sodium in adult patients with acute lung injury (ALI) due to Coronavirus Disease 2019 (COVID-19). This study was designed to determine if dociparstat sodium could accelerate recovery and prevent progression to mechanical ventilation in patients severely affected by COVID-19.

NCT ID: NCT04389450 Terminated - COVID Clinical Trials

Double-Blind, Multicenter, Study to Evaluate the Efficacy of PLX PAD for the Treatment of COVID-19

Start date: October 1, 2020
Phase: Phase 2
Study type: Interventional

This clinical trial will examine if a new treatment of Mesenchymal-like Adherent stromal Cells (called PLX-PAD) can help patients intubated and mechanically ventilated due to COVID-19 to recover more quickly with less complications.

NCT ID: NCT04388683 Terminated - COVID-19 Clinical Trials

Inhaled Nitric Oxide for Preventing Progression in COVID-19

NO-COVID-19
Start date: May 12, 2020
Phase: Phase 2
Study type: Interventional

This is a pilot randomized-controlled (2:1) open label investigation of inhaled NO to prevent progression to more advanced disease in 42 hospitalized patients with COVID-19, at risk for worsening, based on baseline systemic oxygenation and 2 or more of the major risk factors of age > 60 years, type II DM, hypertension, and obesity.

NCT ID: NCT04387448 Terminated - Diabetes Mellitus Clinical Trials

A Study of TRPC5 Channel Inhibitor in Patients With Diabetic Nephropathy, Focal Segmental Glomerulosclerosis, and Treatment-Resistant Minimal Change Disease

Start date: July 28, 2020
Phase: Phase 2
Study type: Interventional

This is a phase 2a study evaluating the safety and tolerability of multiple ascending doses of GFB-887 in patients with diabetic nephropathy (DN), focal segmental glomerulosclerosis (FSGS), and treatment-resistant minimal change disease (TR-MCD).

NCT ID: NCT04387071 Terminated - Clinical trials for Metastatic Pancreatic Adenocarcinoma

CMP-001 and INCAGN01949 for Patients With Stage IV Pancreatic Cancer and Other Cancers Except Melanoma

Start date: April 29, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

This phase Ib/II trial studies the side effects and best dose of CMP-001 and how well it works when given together with INCAGN01949 in treating patients with stage IV pancreatic cancer and other cancers except melanoma. CMP-001 is made up of a short piece of DNA that is packaged in a protein, known as a virus-like particle (VLP). VLPs are detected and processed by cells of the immune system. The DNA contained in CMP-001 activates the immune system and recruit cells of the immune system to the tumor. INCAGN01949 is an antibody, a type of protein, which has been shown to stimulate the immune system. Injecting CMP-001 and INCAGN01949 directly into the tumor may work against tumor cells to slow tumor growth by causing tumor cells to die.

NCT ID: NCT04386811 Terminated - ADHD Clinical Trials

Vitamin D as a Therapeutic Adjunct in the Stimulant Treatment of ADHD: a Proof-of-concept Tele-health Study of Stimulant-induced Improvement in Neurocognitive Functioning.

Start date: August 5, 2020
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess vitamin D as a therapeutic adjunct in the stimulant treatment of ADHD.

NCT ID: NCT04382898 Terminated - Prostate Cancer Clinical Trials

PRO-MERIT (Prostate Cancer Messenger RNA Immunotherapy)

PRO-MERIT
Start date: December 19, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Open-label, multicenter, dose titration and four-arm expansion trial to evaluate the safety, tolerability, immunogenicity, and preliminary efficacy of BNT112 cancer vaccine (BNT112) monotherapy or in combination with cemiplimab in patients with metastatic castration resistant prostate cancer (mCRPC: Part 1 and Part 2 Arms 1A and 1B) and in patients with high-risk, localized prostate cancer (LPC). As of February 2023, the trial will be only recruiting LPC patients and no longer mCRPC patients.

NCT ID: NCT04382391 Terminated - Respiratory Failure Clinical Trials

Study Assessing Vagus Nerve Stimulation in CoViD-19 Respiratory Symptoms

SAVIORII
Start date: May 15, 2020
Phase: N/A
Study type: Interventional

The study is a prospective, randomized, controlled investigation designed for comparison of two groups for the reduction of respiratory distress in a CoViD-19 population, using gammaCore Sapphire (nVNS) plus standard of care (active) vs. standard of care alone (SoC), the control group. The gammaCore® (nVNS) treatments will be used acutely and prophylactically. The aims of this study are to summarize and compare the incidence of clinical events and pro-inflammatory cytokine levels in patients randomized to use of gammaCore Sapphire plus standard of care vs standard of care alone in patients hospitalized for CoViD-19. Secondary objectives are demonstrate the safety of gammaCore Sapphire use in patients hospitalized for CoViD-19.

NCT ID: NCT04381988 Terminated - Cancer Clinical Trials

A Study of Hydroxychloroquine vs Placebo to Prevent COVID-19 Infection in Patients Receiving Radiotherapy

Start date: May 7, 2020
Phase: Phase 2
Study type: Interventional

The researchers are doing this study to find out whether the study drug hydroxychloroquine can prevent infection with the COVID-19 virus, compared with placebo, in people who are receiving radiation therapy for their cancer. The placebo used in this study is a tablet that looks the same as the study drug and is taken in the same way, but it does not contain any active ingredients.

NCT ID: NCT04381494 Terminated - Clinical trials for Unresectable Stage III NSCLC

Mobile Devices to Detect Early Pneumonitis in Stage III NSCLC Patients on Durvalumab.

ON TRAX
Start date: April 27, 2020
Phase: Phase 4
Study type: Interventional

A study of whether mobile devices can improve the detection of pulmonary AEs (including pneumonitis) in stage III NSCLC patients post-CRT, while on durvalumab.