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A Study of ApricityRx™ for Management of IR-AEs in Patients on Immuno-Oncology Therapy

A

Apricity Health

Status

Unknown

Conditions

Cancer

Treatments

Other: ApricityRx mobile application

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

Study of ApricityRx™ for Management of IR-AEs for patients on I-O therapy. Patients currently receiving immunotherapy will be asked to consent to participate in ApricityRx software platform mobile telephone application to report symptoms, view educational content in video form about IO and irAEs and communicate with site study team.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Confirmed cancer diagnosis
  • Prescribed treatment with immune-checkpoint inhibitor
  • Age ≥ 18 years
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion criteria

  • Uncomfortable with or unwilling to use digital or mobile technology
  • Lack of a smart phone with compatible operating systems: iOS version 10 and above, or Android 6.0 Marshmallow
  • Presence of any medical, psychological or social condition that, in the opinion of the investigator, would preclude participation in this study.

Trial contacts and locations

1

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Central trial contact

Research Nurse Navigator

Data sourced from clinicaltrials.gov

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