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NCT ID: NCT03779360 Completed - Inflammation; Skin Clinical Trials

Intradermal LPS and Antibiotics

Start date: October 12, 2018
Phase: N/A
Study type: Interventional

Erythromycin and clindamycin are believed to have anti-inflammatory aspects. This study investigates the possible anti-inflammatory effects of erythromycin and clindamycin.

NCT ID: NCT03777826 Completed - Phenylketonurias Clinical Trials

Effects of Synergy on Nutrient Intake and Acceptability in Phenylketonuria (PKU)

ESSENTIAL
Start date: June 26, 2019
Phase: N/A
Study type: Interventional

Phenylketonuria (PKU) is a rare inherited metabolic disorder, where subjects are born with a genetic deficiency in the phenylalanine hydroxylase enzyme (PAH), which leaves them unable to convert Phenylalanine (Phe) into Tyrosine (Tyr). Patients with mild PKU or partly responsive to the drug synthetic tetrahydrobiopterin (BH4) (Kuvan®) can change to a more relaxed diet. However due to difficulty to adapt their diet, these patients are at risk of an imbalanced nutritional status and an insufficient intake of specific micronutrients, essential amino acids and DHA (Docosahexaenoic acid). The study product is designed to improve the nutritional status of the patients. The study investigates if the nutritional status is indeed improved following 24 week use of the study product, and also the study aims to evaluate product acceptability.

NCT ID: NCT03775499 Completed - Celiac Disease Clinical Trials

Probiotic BL NCC 2705 and Gluten Sensitivity

Start date: October 9, 2018
Phase: N/A
Study type: Interventional

The aim of the study is to confirm/prove safety of the probiotic and production of serpin in humans.

NCT ID: NCT03775200 Completed - Clinical trials for Treatment Resistant Depression

The Safety and Efficacy of Psilocybin in Participants With Treatment Resistant Depression

P-TRD
Start date: March 1, 2019
Phase: Phase 2
Study type: Interventional

The Safety and Efficacy of Psilocybin in Participants with Treatment Resistant Depression

NCT ID: NCT03773068 Completed - Clinical trials for Biological Availability

A Study in Healthy Volunteers Investigating How Quickly and to What Extent BAY1817080 is Taken up, Distributed, Broken Down and Eliminated From the Body, as Well as the Difference Between 2 Different Types of Tablets of BAY1817080 and the Difference Between Oral Dose and Dose in the Vein

Start date: December 13, 2018
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to investigate how quickly and to what extent BAY1817080 is absorbed (taken up), distributed, metabolized (broken down) and eliminated from the body (this is called pharmacokinetics). The pharmacokinetics of BAY1817080 administered as tablets will be compared to the pharmacokinetics of BAY1817080 administered as intravenous (iv; in the vein) infusion (this is called absolute bioavailability). Furthermore, 2 different types of tablets with BAY1817080 (Formulation A and Formulation B) will be compared with regard to pharmacokinetics (this is called relative bioavailability). The effect of a meal on the pharmacokinetics of BAY1817080 administered as tablets will be investigated as well. Finally, it will also be investigated how safe BAY1817080 is and how well BAY1817080 is tolerated.

NCT ID: NCT03772665 Completed - Stargardt Disease Clinical Trials

Safety and Efficacy of Emixustat in Stargardt Disease

SeaSTAR
Start date: January 7, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if emixustat hydrochloride reduces the rate of progression of macular atrophy compared to placebo in subjects with Stargardt disease. Funding Source -- FDA OOPD

NCT ID: NCT03770468 Completed - Glioblastoma Clinical Trials

Molecular Genetic, Host-derived and Clinical Determinants of Long-term Survival in Glioblastoma

Start date: July 5, 2015
Phase:
Study type: Observational

This pro - and retrospective multicenter clinical epidemiological study studies the molecular genetic, host-derived and clinical determinants of glioblastoma patients with an overall survival of more than 5 years. The different research focusses are: - Identification of clinical parameters and patient characteristics / host-related factors in long-term survivors (Focus 1) - Identification of molecular tumor characteristics in long-term survivors (Focus 2) - Assessment of therapy-related parameters, including neuro-toxicity (Focus 3) - Immunological studies (Focus 4)

NCT ID: NCT03770403 Completed - Clinical trials for Generalized Myasthenia Gravis

A Safety and Tolerability Study of ARGX-113 in Patients With Myasthenia Gravis Who Have Generalized Muscle Weakness.

ADAPT+
Start date: March 1, 2019
Phase: Phase 3
Study type: Interventional

This is a Long-Term, Single-Arm, Open-Label, Multicenter Phase 3 follow-on trial of the ARGX-113-1704 study to evaluate the safety and tolerability of ARGX-113 in patients with gMG. Patients who have completed at least 1 cycle of treatment and at least 1 year of trial ARGX-113-1705 and have started Part B are eligible to enroll in the open-label trial ARGX-113-2002 to receive efgartigimod by SC administration.

NCT ID: NCT03770039 Completed - Clinical trials for Healthy Male Subjects

Single Dose Study With Unlabeled Dose and 14C-labeled Microdose of PF-06700841 in Healthy Male Subjects

Start date: December 10, 2018
Phase: Phase 1
Study type: Interventional

An open-label, fixed sequence, 2-period including a single oral dose 60 mg PF-06700841 with 14C-labeled microtracer in 1st period, and a single oral dose of 60 mg unlabeled PF-06700841 followed by intravenous administration of 14C-labeled microdose of PF-06700841 1 hour after oral dose in period 2 to characterize the absorption, disposition, metabolism and excretion of PF-06700841 and evaluate the absolute bioavailability and fraction absorbed in the GI tract

NCT ID: NCT03768089 Completed - Cystic Fibrosis Clinical Trials

Study of VX-121 in Healthy Subjects and in Subjects With Cystic Fibrosis

Start date: March 20, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate safety and tolerability of VX-121 in healthy subjects and in subjects with cystic fibrosis (CF).