Actively Recruiting

Phase 2
Age: 18Years +
FEMALE
NCT04918186

Immunotherapy Platform Study in Platinum Resistant High Grade Serous Ovarian Cancer

Led by Canadian Cancer Trials Group · Updated on 2026-05-12

60

Participants Needed

7

Research Sites

243 weeks

Total Duration

On this page

Sponsors

C

Canadian Cancer Trials Group

Lead Sponsor

C

Cancer Research Institute, New York City

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study is being done to answer the following question: What are the effects of a new drug or drugs on ovarian cancer? The pre-study screening may be done to test a sample of tissue for biomarkers to determine participation in the study.

CONDITIONS

Official Title

Immunotherapy Platform Study in Platinum Resistant High Grade Serous Ovarian Cancer

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women with platinum resistant high grade serous ovarian, fallopian tube, or peritoneal carcinoma
  • Disease progression within 6 months of last platinum chemotherapy
  • Measurable disease by RECIST 1.1 criteria
  • At least one disease site suitable for pre and on-treatment biopsies
  • At least 28 days since any major surgery with healed wounds
  • No more than one prior cytotoxic chemotherapy regimen for platinum-resistant disease
  • Prior immune checkpoint inhibitor allowed if discontinued without severe toxicity
  • Minimum 4 weeks since last therapy with recovery from toxicity to grade 1 or less
  • Radiation, endocrine, or non-anti-cancer investigational agents allowed with 28 day gap
  • ECOG performance status 0 or 1 and life expectancy 3 months or more
  • Age 18 years or older
  • Consent for tumor tissue release and biopsies
  • Willing and able to comply with study visits, treatment, and tests
  • Adequate organ and marrow function within 7 days prior to enrollment
  • Signed informed consent
  • Accessible for treatment and follow-up at participating center
  • Protocol treatment to begin within 2 working days of enrollment
  • Negative pregnancy test for women of childbearing potential
Not Eligible

You will not qualify if you...

  • History of other malignancies affecting safety or efficacy unless curatively treated
  • Uncontrolled or serious illnesses posing safety risks, including recent intra-abdominal abscess, active infections, HIV, hepatitis B or C with detectable viral load
  • History of interstitial lung disease or severe pulmonary disease
  • Significant pleural, pericardial, or peritoneal effusions requiring intervention
  • Autoimmune diseases requiring chronic steroids
  • Stroke or transient ischemic attack within 6 months
  • Significant cardiac disease within 6 months
  • Prior allogeneic stem cell or organ transplantation
  • Central nervous system metastases that are symptomatic or uncontrolled
  • Pregnant or breastfeeding women
  • Concurrent treatment with other anti-cancer or investigational agents
  • Active or recent autoimmune or inflammatory disorders within past 3 years, except select low-risk conditions
  • Live vaccine administration within 4 weeks prior to enrollment
  • QTc interval above specified thresholds or with additional risk factors

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

The University of Chicago Medical Center

Chicago, Illinois, United States, 60637

Actively Recruiting

2

BCCA - Kelowna

Kelowna, British Columbia, Canada, V1Y 5L3

Not Yet Recruiting

3

BCCA - Vancouver

Vancouver, British Columbia, Canada, V5Z 4E6

Not Yet Recruiting

4

Odette Cancer Centre

Toronto, Ontario, Canada, M4N 3M5

Not Yet Recruiting

5

University Health Network

Toronto, Ontario, Canada, M5G 2M9

Not Yet Recruiting

6

CHUM-Centre Hospitalier de l'Universite de Montreal

Montreal, Quebec, Canada, H2X 3E4

Not Yet Recruiting

7

The Jewish General Hospital

Montreal, Quebec, Canada, H3T 1E2

Not Yet Recruiting

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Research Team

J

Janet Dancey

CONTACT

P

Pierre-Olivier Gaudreau

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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Immunotherapy Platform Study in Platinum Resistant High Grade Serous Ovarian Cancer | DecenTrialz