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Adults with T2DM of 7 years on 0-2 anti-diabetic drugs, including glargine and pre-meal insulin lispro will be randomized to 8 weeks of therapy with either basal insulin glargine, intensive insulin therapy consisting of glargine and pre-meal insulin lispro, or glargine and the GLP-1 agonist exenatide.
Source link: https://clinicaltrials.gov/ct2/show/NCT02194595
Patients will be randomized to either oral ladarixin therapy or placebo. Both Ladarixin and placebo will be administered for 1 year. From the 1st administration of the study drugs, all patients will be followed-up for 18 months. When the last patient randomized has completed the month 12 follow-up visit, the research database will be locked and results will be analyzed.
Source link: https://clinicaltrials.gov/ct2/show/NCT04899271
It has been developed to investigate whether ladarixin is safe in preserving beta-cell function and slowing-down the development of T1D in patients with a more severe disease course. The Principal Investigator PI, the protocol, GCP guidelines, and local rules would all be responsible for ensuring that the investigation is carried out according to the signed Investigator deal, the protocol, GCP guidelines, and local policies. For 13 cycles of 14 days on/14 days off, placebo control group or matched placebo control group, a treatment group or matched placebo control group was compared.
Source link: https://clinicaltrials.gov/ct2/show/NCT04628481
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