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NCT ID: NCT05094674 Recruiting - COVID-19 Clinical Trials

Clinical Validation of Breath Analyser Tests for Diagnosis of COVID-19.

Start date: October 22, 2021
Phase: N/A
Study type: Interventional

The Sponsor has developed a rapid screening tool intended to determine if the subject tested is COVID-19-free (Negative to COVID-19).

NCT ID: NCT05094336 Recruiting - Clinical trials for Advanced MTAP-null Solid Tumors

AMG 193, Methylthioadenosine (MTA) Cooperative Protein Arginine Methyltransferase 5 (PRMT5) Inhibitor, Alone and in Combination With Docetaxel in Advanced Methylthioadenosine Phosphorylase (MTAP)-Null Solid Tumors

MTAP
Start date: February 1, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of Parts 1 and 2 of this study is to evaluate the safety, tolerability, and to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) of AMG 193 alone and in combination with docetaxel in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-null solid tumors. The primary objective of Part 3 of this study is to evaluate the objective response rate (ORR) of AMG 193 in adult participants with metastatic or locally advanced MTAP-null solid tumors.

NCT ID: NCT05094089 Recruiting - Hernia, Ventral Clinical Trials

Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application

SYN 20-01
Start date: February 24, 2023
Phase:
Study type: Observational

The SYN 20-01 Study is a non-interventional, prospective, multicenter, multicohort, international, post-market clinical investigation looking into the assessment of GORE® SYNECOR Biomaterial in focused patient populations and in long-term application. Patients with ventral / incisional hernia amenable to hernia mesh repair will be enrolled into two cohorts (US and EU cohort) and followed-up over the period of 60 months.

NCT ID: NCT05093634 Recruiting - Obesity Clinical Trials

EMANATE: A Study of Setmelanotide in Patients With Specific Gene Variants in the MC4R Pathway

Start date: December 10, 2021
Phase: Phase 3
Study type: Interventional

The protocol describes a randomized, double-blind, placebo-controlled trial with independent sub-studies of setmelanotide in patients with obesity and at least one of the specific gene variants in the Melanocortin-4 Receptor pathway: - POMC or PCSK1 (Sub-study 035a) - LEPR (Sub-study 035b) - SRC1 (Sub-study 035c) - SH2B1 (Sub-study 035d) The objectives and endpoints are identical for these sub-studies.

NCT ID: NCT05092685 Recruiting - Clinical trials for Ornithine Transcarbamylase Deficiency

Halting Ornithine Transcarbamylase Deficiency With Recombinant AAV in ChildrEn

HORACE
Start date: November 1, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

Ornithine transcarbamylase deficiency (OTCD) is an inherited metabolic liver disease which means that the body cannot maintain normal levels of ammonia. Ammonia levels can rise (called hyperammonaemic decompensations) which can be life-threatening and may result in impaired neurological development in children. OTCD is a rare genetic disorder characterised by complete or partial lack of the enzyme ornithine transcarbamylase (OTC).

NCT ID: NCT05092399 Recruiting - Obesity Clinical Trials

Effects of VLCD and Bariatric Surgery in Patients With Type 2 Diabetes

BARIATRICMRI
Start date: July 1, 2022
Phase:
Study type: Observational

The investigators are therefore interested to explore the effects of VLCD and different bariatric surgery procedures to changes in the physical deposition of fat in organs which regulate glucose metabolism (i.e. in the liver, pancreas, muscle) in the earlier (6 weeks) and intermediate (4 months) period after bariatric surgery, where rate of weight loss at this stage are similar between the two procedures. Increased understanding of the changes in these important metabolic organs, will increase the investigators' understanding of mechanism of diabetes remission following bariatric surgery, their effects on weight loss or changes in gut hormones levels. Magnetic Resonance imaging (MRI) and Magnetic Resonance spectroscopy (MRS) are non-invasive, non-ionising techniques. MRI can be used to investigate the body's physiology and MRS can be used to investigate the body's metabolic processes, so by combining these two methods the investigators are able to investigate the process of fat reduction and diabetes remission post gastric surgery without performing any secondary invasive procedures The purpose of this project is to investigate the effects of a Very Low Calorie Diet (VLCD) followed by two different bariatric surgical procedures, Roux-en-Y Gastric Bypass (RYGB) and Sleeve gastrectomy (SG) on skeletal muscle, liver and pancreatic fat deposition, ATP flux as well as cardiac function.

NCT ID: NCT05092360 Recruiting - Clinical trials for Fallopian Tube Cancer

Phase 3 Study of Nemvaleukin Alfa in Combination With Pembrolizumab in Patients With Platinum-Resistant Epithelial Ovarian Cancer (ARTISTRY-7)

ARTISTRY-7
Start date: January 10, 2022
Phase: Phase 3
Study type: Interventional

This is a Phase 3, multicenter, open-label, randomized study of nemvaleukin in combination with pembrolizumab versus protocol-specific Investigator's choice chemotherapy in patients with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer.

NCT ID: NCT05092269 Recruiting - Crohn Disease Clinical Trials

A Long-term Extension Study of Ustekinumab in Pediatric Participants

UNITED
Start date: October 18, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to collect long-term safety data of subcutaneous (SC) ustekinumab

NCT ID: NCT05091424 Recruiting - Clinical trials for Chronic Lymphocytic Leukemia

A Study Evaluating the Safety, Efficacy, and Pharmacokinetics of Mosunetuzumab and a Combined Regimen of Mosunetuzumab and Venetoclax in Participants With Relapsed or Refractory Chronic Lymphocytic Leukemia

Start date: March 7, 2022
Phase: Phase 1
Study type: Interventional

This study will assess the safety, tolerability, pharmaokinetics, and preliminary efficacy of mosunetuzumab (Lunsumio) monotherapy in participants with relapsed or refractory (R/R) chronic lymphocytic leukemia (CLL). This study will also allow participants who are currently progressing on a Bruton tyrosine kinase inhibitor (BTKi) and requiring salvage therapy as assessed by the treating physician to continue their BTKi throughout the screening period and for the first two cycles of mosunetuzumab. An additional arm has been added to assess the safety, tolerability, pharmacokinetics, and preliminary efficacy of mosunetuzumab in combination with venetoclax, a B-cell lymphoma 2 (BCL2) inhibitor.

NCT ID: NCT05091112 Recruiting - Nerve Degeneration Clinical Trials

Nerve Composition of Human Lumbar Dorsal Primary Rami and Its Medial Branch

Start date: March 8, 2022
Phase:
Study type: Observational

The purpose of the study is to understand the composition of the nerves supplying the facet joints in low back.