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NCT ID: NCT05165433 Recruiting - Metastatic Cancer Clinical Trials

Study of NG-350A Plus Pembrolizumab in Metastatic or Advanced Epithelial Tumours (FORTIFY)

FORTIFY
Start date: April 13, 2022
Phase: Phase 1
Study type: Interventional

This is a phase 1a/1b, multicentre, open-label, non-randomized study of NG-350A in combination with pembrolizumab in patients with metastatic or advanced epithelial tumours.

NCT ID: NCT05237440 Recruiting - Obesity Clinical Trials

Childhood Traumas in Obese Women: Association With Deregulation of the Glucocorticoid Axis and Inflammatory State.

OBEVIE
Start date: April 13, 2022
Phase: N/A
Study type: Interventional

We postulate that childhood traumas are associated with deregulation of the glucocorticoid axis and the inflammatory system in obese women. The main objective of the study is to compare the salivary cortisol awaking response in obese women according to the presence of childhood trauma (assessed using the Childhood Trauma Questionnaire, CTQ).

NCT ID: NCT05243290 Recruiting - Gulf War Illness Clinical Trials

Nicotinamide Riboside Clinical Trial for GWI

Start date: April 13, 2022
Phase: N/A
Study type: Interventional

In this multi-site trial, we will use a randomized, double-blind, placebo-controlled study design to test whether 300 mg of Nicotinamide Riboside (NR) can achieve the primary objective of increasing plasma NAD+ levels in participants with Gulf War Illness (GWI).

NCT ID: NCT05243563 Recruiting - Clinical trials for Vulvar Lichen Sclerosus

Does Steroid Plus CO2 Laser Improve Lichen Sclerosus Symptoms Compared to Steroids Alone?

Start date: April 13, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

This study will compare the effects of fractionated CO2 laser plus topical steroids versus topical steroids alone in treatment of lichen sclerosus.

NCT ID: NCT05253053 Recruiting - Prostate Cancer Clinical Trials

To Evaluate Efficacy and Safety of TT-00420 (Tinengotinib) as Monotherapy and Combination Therapy in Patients With Advanced Solid Tumors

Start date: April 13, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase Ib/II, multicenter, open-label study to evaluate the safety and preliminary efficacy of TT-00420 tablet, as monotherapy or in combination regimens, in patients with advanced solid tumors (solid tumor, BTC and TNBC).

NCT ID: NCT05254795 Recruiting - Clinical trials for Non-Small Cell Lung Cancer

Precision Medicine Randomized Clinical Trial Comparing Molecular Tumor Board Assisted Care to Usual Care

PRiMAL
Start date: April 13, 2022
Phase: N/A
Study type: Interventional

This trial will compare Molecular Tumor Board (MTB) assisted care to usual care for patients who have newly diagnosed histologically or cytologically confirmed stage IIb-IV Non-Small Cell Lung Cancer (NSCLC) and are planning to undergo treatment for their cancer.

NCT ID: NCT05257473 Recruiting - Clinical trials for Muscular Dystrophies

Defining Endpoints in Becker Muscular Dystrophy

GRASP-01-002
Start date: April 13, 2022
Phase:
Study type: Observational

This is a 24-month, observational study of 50 participants with Becker muscular dystrophy (BMD)

NCT ID: NCT05266495 Recruiting - Clinical trials for Neovascular Age-related Macular Degeneration

Effectiveness of Brolucizumab in Pre-treated Patients With nAMD in the Real-world Setting

Start date: April 13, 2022
Phase:
Study type: Observational

The study is a prospective and retrospective, observational, single-arm, non-randomized cohort study of ocular treatment with intravitreal injections of brolucizumab in nAMD patients. This study will be conducted prospectively and retrospectively (for patients who had their first brolucizumab injection before study start) using data collected in a standardized manner.

NCT ID: NCT05276804 Recruiting - Clinical trials for Postoperative Urinary Retention

The POUR (Postoperative Urinary Retention) Study

POUR
Start date: April 13, 2022
Phase: Phase 3
Study type: Interventional

The primary aim of this study will be to compare the rate of postoperative urinary retention between patients receiving Sugammadex and those receiving traditional reversal agents

NCT ID: NCT05278715 Recruiting - Optic Glioma Clinical Trials

Modified CV Regimen in Optic Pathway Glioma

Start date: April 13, 2022
Phase: Phase 2
Study type: Interventional

Optic pathway glioma (OPG) can result in visual deterioration. Symptomatic patients often report deficits in visual acuity (VA), visual field, visual-evoked potentials (VEPs), strabismus, proptosis, disc swelling, and other visual/neurological problems. VA itself remains one of the most important outcome measures for OPG patients, with various studies showing strong ties of VA level to overall quality of life and well-being . Maintenance of favorable VA and vision outcomes is of paramount importance in the management of OPG. In terms of management of OPG, surgery and radiotherapy are used on a more limited basis because of location of the tumors and risk of secondary tumors, respectively. Tumor stabilization often prioritized, and chemotherapy is considered ideal for tumor stabilization in OPG, but vision is not always retained and may worsen in some cases, partially due to low radiographic efficacy and long time interval to response of the current chemotherapy regimen. In the prior study, the investigators modified the traditional carboplatin combined with vincristine regimen by increasing the dose of carboplatin and combining with an anti-angiogenic drug. Of the 15 OPG patients, objective response rate was 80% and the time to response was only 3.3 months. 8 (53%) patients experienced an improvement in visual acuity during therapy and 6 (40%) were stable, which was higher than the historical studies. This study was launched to further verify the clinical efficacy of the modified regimen and its effect on visual acuity improvement.