Dr. Cassandra C. Key

Geriatrics
Ipc Healthcare Services Of Texas PLLC
7330 San Pedro Ave Ste 540, 
San Antonio, TX 
Accepting New Patients
Ipc Healthcare Services Of Texas PLLC
7330 San Pedro Ave Ste 540, 
San Antonio, TX 

Overview

Cassandra Key is a Geriatrics provider practicing medicine in San Antonio, Texas.

She is actively involved in clinical research, co-authoring 5 peer reviewed articles and participating in 7 clinical trials. Dr. Key is currently accepting new patients.

Specialties

Geriatrics

Licenses

Internal Medicine in TX

Languages Spoken

English

Gender

Female

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Aetna
  • EPO
  • HMO
  • POS
  • PPO
Blue Cross Blue Shield
  • EPO
  • HMO
  • POS
  • PPO
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
Medicaid
  • OTHER MEDICAID
  • STATE MEDICAID
Oscar
  • EPO
  • HMO
  • PPO

Locations

Ipc Healthcare Services of Texas PLLC
7330 San Pedro Ave Ste 540, San Antonio, TX 78216

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

7 Clinical Trials

A Phase 1, Double-Blind, Placebo-Controlled, Single Ascending Dose Study in Healthy Volunteers to Evaluate the Safety, Tolerability, and Pharmacokinetics of RGLS8429
A Phase 1, Double-Blind, Placebo-Controlled, Single Ascending Dose Study in Healthy Volunteers to Evaluate the Safety, Tolerability, and Pharmacokinetics of RGLS8429
Enrollment Status: Completed
Publish Date: August 27, 2025
Intervention Type: Drug
Study Phase: Phase 1
A Phase 1, Randomized, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and PK of LY3541105 Following Single Doses in Healthy/Overweight Participants and Multiple Doses in Overweight Participants
A Phase 1, Randomized, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and PK of LY3541105 Following Single Doses in Healthy/Overweight Participants and Multiple Doses in Overweight Participants
Enrollment Status: Completed
Publish Date: June 27, 2025
Intervention Type: Drug
Study Phase: Phase 1
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety, Pharmacokinetics, and Immunogenicity of ADM03820 in Adults
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety, Pharmacokinetics, and Immunogenicity of ADM03820 in Adults
Enrollment Status: Completed
Publish Date: March 07, 2025
Intervention Type: Other, Drug
Study Drug: ADM03820 Anti-COVID-19 Vaccine
Study Phase: Phase 1
CSD190202: A Randomized, Open-Label, Crossover Study to Assess Elements of Abuse Liability for Two Electronic Nicotine Delivery Systems
CSD190202: A Randomized, Open-Label, Crossover Study to Assess Elements of Abuse Liability for Two Electronic Nicotine Delivery Systems
Enrollment Status: Completed
Publish Date: June 27, 2022
Intervention Type: Other
Study Phase: Not Applicable
A Phase 1b, Multicenter, Open-Label, Adaptive Design Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RGLS4326 Administered Via SC Injection to Patients With Autosomal Dominant Polycystic Kidney Disease
A Phase 1b, Multicenter, Open-Label, Adaptive Design Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RGLS4326 Administered Via SC Injection to Patients With Autosomal Dominant Polycystic Kidney Disease
Enrollment Status: Completed
Publish Date: December 15, 2021
Intervention Type: Drug
Study Drug: RGLS4326
Study Phase: Phase 1
A Multi-Center, Randomized, Placebo-Controlled, Phase 1, Two-Part Study Designed to Assess the Safety, Tolerability, Pharmacokinetics, Food Effect, and Drug-Drug Interactions of PTI-801 in Healthy Volunteers, and Safety, Tolerability, and Pharmacokinetics of PTI-801 in Subjects With Cystic Fibrosis
A Multi-Center, Randomized, Placebo-Controlled, Phase 1, Two-Part Study Designed to Assess the Safety, Tolerability, Pharmacokinetics, Food Effect, and Drug-Drug Interactions of PTI-801 in Healthy Volunteers, and Safety, Tolerability, and Pharmacokinetics of PTI-801 in Subjects With Cystic Fibrosis
Enrollment Status: Completed
Publish Date: April 30, 2020
Intervention Type: Drug
Study Phase: Phase 1
Comparative Pharmacokinetics and Food-Effect Bioavailability of a Sprinkle Formulation of Lubiprostone After Oral Administration in Healthy Volunteers
Comparative Pharmacokinetics and Food-Effect Bioavailability of a Sprinkle Formulation of Lubiprostone After Oral Administration in Healthy Volunteers
Enrollment Status: Completed
Publish Date: March 09, 2020
Intervention Type: Drug
Study Phase: Phase 3
View 6 Less Clinical Trials

5 Total Publications

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the Novel Long-Acting FGF21 Analog Zalfermin.
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the Novel Long-Acting FGF21 Analog Zalfermin.
Journal: Clinical and translational science
Published: July 07, 2025
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Frequently Asked Questions about Dr. Cassandra C. Key

How do I make an appointment with Dr. Cassandra C. Key?

You can book an appointment with Dr. Cassandra C. Key by calling their office at 210-344-7287. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.

Does Dr. Cassandra C. Key accept my insurance?

Dr. Cassandra C. Key accepts most major insurance plans, including Aetna and Blue Cross Blue Shield. We recommend calling the office directly at 210-344-7287 to verify that your specific plan is currently accepted before your visit.

Areas of Expertise

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