The goal of this clinical trial is to evaluate the potential of Calcium Hydroxylapatite (CaHA) to restore facial volume and improve skin quality in patients with GLP-1 receptor agonist-associated facial volume loss. Participants will: * Schedule first dose of a prescribed GLP-1 receptor agonist drug to coincide with the baseline visit of this study * Be randomly assigned to one of two groups (Group A will receive off-label injections of hyperdiluted CaHA at Month 0. Group B will receive on-label injections of CaHA after serving as a control group through Month 6) * Have clinical photos taken at each office visit to track progress
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Change in Cheek Volume, as quantified by Quantificare's LifeViz Software
Timeframe: Up to 6 months
Change in Jowl Volume, as quantified by Quantificare's LifeViz Software
Timeframe: Up to 6 months
Change in Nasolabial Fold Depth, as quantified by Quantificare's LifeViz Software
Timeframe: Up to 6 months
Change in Marionette Line Depth, as quantified by Quantificare's LifeViz Software
Timeframe: Up to 6 months
Body Mass Index (BMI)
Timeframe: Up to 12 months
Global Aesthetic Improvement Scale (GAIS) for Global Facial Aesthetic Appearance
Timeframe: Up to 6 months
Global Aesthetic Improvement Scale (GAIS) for Skin Quality
Timeframe: Up to 6 months
Global Aesthetic Improvement Scale (GAIS) for Skin Radiance
Timeframe: Up to 6 months