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OHR/AVR118 for Cancer Cachexia

Phase 2
Waitlist Available
Led By Martin Chasen, MBChB
Research Sponsored by Ohr Pharmaceutical Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks
Awards & highlights

Study Summary

The purpose of this study is to determine whether patients with advanced cancers who receive OHR/AVR118 solution for injection into the skin can achieve improvement in quality of life. Based on a previous study in patients with AIDS, possible benefits may include improved appetite and strength; weight gain, improved mood; and decreased fatigue.

Eligible Conditions
  • Cancer Cachexia
  • Anorexia

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~four weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and four weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Alleviation of multiple cachexia symptoms
Secondary outcome measures
Corticotropin

Trial Design

1Treatment groups
Experimental Treatment
Group I: OHR/AVR118Experimental Treatment1 Intervention
Experimental Drug

Find a Location

Who is running the clinical trial?

Ohr Pharmaceutical Inc.Lead Sponsor
5 Previous Clinical Trials
392 Total Patients Enrolled
Martin Chasen, MBChBPrincipal InvestigatorOttawa Hospital Cancer Centre

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~1 spots leftby May 2025