Pilot Study of Bone Mineral Density Changes During Anti-PD-1 Immunotherapy
NCT07555210
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment and work by blocking protein interactions that normally prevent the immune system from recognizing and destroying cancer cells. However, these agents, now approved for over 15 types of cancers and for both early-stage and metastatic disease, are capable of causing inflammation in any organ system of the body that can lead to organ damage, dysfunction, and even death in rare cases.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Breast Cancer (Triple Negative Breast Cancer (TNBC))
- Renal Cell Carcinoma (Kidney Cancer)
- Melanoma (Skin Cancer)
- Non-Small Cell Lung Cancer
- MSI-H/dMMR Rectal Cancer
- Squamous Cell Carcinoma Mouth
- Invasive Mammary Carcinoma
- Classic Hodgkin Lymphoma
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Jessica Mezzanotte Sharpe
- Last updated on ClinicalTrials.gov
- May 6, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Tennessee · 1
- Vanderbilt-Ingram Cancer Center · Nashville, TN
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.