Clinical Trials Directory

Trials / Completed

CompletedNCT05675111

Immune Checkpoint Inhibitors(ICPis)-Induced Endocrine Immune-related Adverse Events (irAEs)

Endocrine-related Adverse Events Caused by Immune Checkpoint Inhibitors

Status
Completed
Phase
Study type
Observational
Enrollment
12,408 (actual)
Sponsor
Nanjing Medical University · Academic / Other
Sex
All
Age
18 Years – 88 Years
Healthy volunteers
Not accepted

Summary

Immune checkpoint inhibitor (ICI) includes agents that block cytotoxic T-cell-associated antigen 4 (CTLA-4), programmed cell death protein 1 (PD-1), and programmed cell death protein ligand 1 (PD-L1). Since the FDA-approval of the CTLA-4 inhibitor ipilimumab in 2011, ICI drugs have emerged as a powerful new tool in the treatment for several advanced cancers. Now indications for ICI have expanded dramatically due to their efficacy and include a wide array of cancer types. However, the administration of ICI, whereas, carry the risk of developing immune-related adverse events (irAEs) and may lead to serious and even fatal events. Endocrine dysfunctions are among the most common irAEs that have been reported in clinical trials with ICI, including thyroid dysfunction, hypopituitarism, primary adrenal insufficiency (PAI) and insulin-deficient diabetes (ICI-DM). However, it is difficult to acquire a complete picture of irAEs from randomized controlled trials (RCTs) due to limitations in the study design and realistic practicalities.

Conditions

Timeline

Start date
2018-06-01
Primary completion
2022-03-31
Completion
2022-10-30
First posted
2023-01-09
Last updated
2023-01-09

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05675111. Inclusion in this directory is not an endorsement.