ORB-021 In Patients With Advanced Solid Tumors

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorOrionis Biosciences Inc

About this trial

The goal of this clinical research study is to determine if an investigational new drug, named ORB-021, developed by Orionis Biosciences is safe and can be tolerated in people diagnosed with an advanced solid tumor.

The study also aims to find the biologically optimal dose of the study medicine by assessing the safety and potential activity in the treatment of solid tumors.

There are three phases to this study: screening, treatment and end of treatment.

Eligibility criteria

Qualifiers

Age 18 years or older

Patients with evidence of recurrent or refractory solid tumors deemed medically safe to undergo serial biopsies.

Must have received or be ineligible for all standard of care therapies as deemed appropriate by the treating physician.

Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1

Disqualifiers

Patients who are receiving any other investigational agents

History of allergic reactions attributed to compounds of similar chemical or biologic composition to ORB-021 or its excipients.

Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. Urinary tract infections (UTIs) are excluded from being an exclusion criterion for treatment unless they are Grade 3 or higher.

Pregnant women are excluded from this study because the effects of ORB-021 on a pregnant woman or fetus are unknown. Breastfeeding should be discontinued as the potential risk for AEs in nursing infants treated with ORB-021 is unknown.

Trial design

Treatments tested in this trial

  • ORB-021

Treatment groups

36 Participants
are divided into 1 treatment group

Sponsors and collaborators