Hepatocyte Nuclear Factor 1-beta

Clinical trial pipeline · Data from ClinicalTrials.gov

See which Hepatocyte Nuclear Factor 1-beta trials you may qualify for

Total trials

Actively recruiting

Phase 3 trials

Completed

Trial phase breakdown

Trial status

Actively recruiting — 1 trial

RecruitingNot Applicable

NCT06065852

National Registry of Rare Kidney Diseases

The goal of this National Registry is to is to collect information from patients with rare kidney diseases, so that it that can be used for research. The purpo…

United Kingdom35,000 participantsStarted 2009-11-06

All recent trials (4 shown)

CompletedNot Applicable

NCT04746053

Ovarian Function and Gynecological Profile of Patients Carrying a Pathogenic Variant of the HNF1B Gene (GYN-HNF1)

The main objective of this study is to study the ovarian function of patients with hepatocyte nuclear factor-1beta (HNF1B) abnormality, followed in the referenc…

France26 participantsStarted 2021-04-12

Treatment: Pelvic ultrasound, blood sample

UnknownPhase 4

NCT04239586

Switching From Insulin to Sulfonylurea in Diabetes Associated With Variants in MODY Genes

The purpose of this study is to switch from insulin to oral sulfonylurea in patients with apparent type 1 diabetes or maturity onset diabetes in the young that…

Norway30 participantsStarted 2017-04-18

Treatment: Sulfonylurea

Hepatocyte Nuclear Factor 1-beta

Trial phase breakdown

Trial status

Actively recruiting — 1 trial

National Registry of Rare Kidney Diseases

All recent trials (4 shown)

Ovarian Function and Gynecological Profile of Patients Carrying a Pathogenic Variant of the HNF1B Gene (GYN-HNF1)

Switching From Insulin to Sulfonylurea in Diabetes Associated With Variants in MODY Genes

Trial phase breakdown

Trial status

Actively recruiting — 1 trial

National Registry of Rare Kidney Diseases

All recent trials (4 shown)

Ovarian Function and Gynecological Profile of Patients Carrying a Pathogenic Variant of the HNF1B Gene (GYN-HNF1)

Switching From Insulin to Sulfonylurea in Diabetes Associated With Variants in MODY Genes

Long Term Follow up of a Cohort of Children With TCF2 Mutation:Evolution of Endocrine and Renal Function