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Looking for participantsPhase2

A Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression

Sponsor: Incyte Corporation

NCT ID: NCT07023627

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
INCB123667 (drug)
How long the study runs
Study runs about 23 months (dates as stated)
About the drug or intervention
INCB123667 — drug: Administered orally twice daily (BID).
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years to 99 Years
Who
Female
Number of participants
160
Started
2025-11-12
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for ovarian cancer
  • • Phase2 - 160 participants
  • • This study will evaluate the safety and efficacy of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer (PROC) With Cyclin E1 Overexpression

Who can take part?

  • • Ages 18 Years to 99 Years
  • • Diagnosed with ovarian cancer
  • • Female only

Where?

  • • London - Guy'S Hospital - Guy'S & St Thomas' Nhs Foundation Trust
  • • London - Royal Marsden Hospital (Sutton) - Royal Marsden Nhs Foundation Trust
  • • London - Hammersmith Hospital - Imperial College Healthcare Nhs Trust
  • • Manchester Greater - The Christie Nhs Foundation Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

This study will evaluate the safety and efficacy of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer (PROC) With Cyclin E1 Overexpression.

Ovarian Cancer

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years - 99 Years
  • Who can join: Female only

Biomarkers mentioned

tests positivePR

Treatment history

Treatments you must have had:

  • ✓ received at least 4 cycles of a platinum-containing regimen
  • ✓ progressed on or within 6 months after the last dose of platinum
  • ✓ received bevacizumab unless there was a contraindication for its use
  • ✓ received mirvetuximab soravtansine unless there is an exception for its use on medical grounds

What the study is looking for

  • ✓Histological diagnosis of a high-grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer.
  • ✓Have platinum-resistant disease:
  • ✓Participants who have only had 1 line of platinum-based therapy must have received at least 4 cycles of a...
  • ✓Participants who have received 2 to 4 lines of platinum-based therapy must have progressed on or within 6 months...
  • ✓Willingness to undergo a pretreatment biopsy. Note: Tissue from a fresh pretreatment biopsy is preferred, however an...

Who cannot take part

  • ✗Have endometrioid, clear cell, mucinous, or sarcomatous histology, mixed tumors containing any of these histologies,...
  • ✗The tumor tests positive for FRα but the participant has not received mirvetuximab soravtansine for any reason other...
  • ✗Clinically significant or uncontrolled heart disease within 6 months before the first dose of the study treatment.
  • ✗Known active CNS metastases and/or carcinomatous meningitis.
  • ✗Known additional cancer that is progressing or requires active treatment.
See the full criteria
Inclusion Criteria: * Histological diagnosis of a high-grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer. * Have platinum-resistant disease: * Participants who have only had 1 line of platinum-based therapy must have received at least 4 cycles of a platinum-containing regimen. * Participants who have received 2 to 4 lines of platinum-based therapy must have progressed on or within 6 months after the last dose of platinum. * Willingness to undergo a pretreatment biopsy. Note: Tissue from a fresh pretreatment biopsy is preferred, however an archival sample is acceptable as long as the sample is no older than 5 years. * Received at least 1 and no more than 4 prior lines of systemic therapy following the initial diagnosis, after which single-agent therapy is considered an appropriate next therapeutic option. * Must have received bevacizumab unless there was a contraindication for its use. * If the tumor tests positive for FRα, participants must have received mirvetuximab soravtansine unless there is an exception for its use on medical grounds. Exclusion Criteria: * Have endometrioid, clear cell, mucinous, or sarcomatous histology, mixed tumors containing any of these histologies, or low-grade/borderline ovarian cancer. * Have primary platinum-refractory disease: either did not respond (CR or PR) to first-line platinum-containing therapy or progressed on or within 3 months after the last dose of the first line platinum-containing therapy. * The tumor tests positive for FRα but the participant has not received mirvetuximab soravtansine for any reason other than medical contraindication. * Clinically significant or uncontrolled cardiac disease within 6 months before the first dose of study drug. * Known active CNS metastases and/or carcinomatous meningitis. * Known additional malignancy that is progressing or requires active treatment. Other protocol-defined Inclusion/Exclusion Criteria may apply.

Where Is This Study? (4 UK sites)

Guy'S Hospital - Guy'S & St Thomas' Nhs Foundation Trust

London SE1 9RT, United Kingdom

Recruiting
Hospital R&D contact (matched)

Main Email: gstt.RandD@nhs.net

gstt.RandD@nhs.net---

Royal Marsden Hospital (Sutton) - Royal Marsden Nhs Foundation Trust

London SM2 5PT, United Kingdom

Recruiting
Hospital R&D contact (matched)

Mark Brandon-Grove

research.development@rmh.nhs.uk020 3186 5416

Hammersmith Hospital - Imperial College Healthcare Nhs Trust

London W12 0HS, United Kingdom

Recruiting
Hospital R&D contact (matched)

Donna Copeland

donna.copeland@nhs.net---

The Christie Nhs Foundation Trust

Manchester Greater M204BX, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Innovation Office

the-christie.ri@nhs.net---

How to Get in Touch

Incyte Corporation Call Center (US)

Sponsor contact

CONTACT

1.855.463.3463 medinfo@incyte.com

Incyte Corporation Call Center (ex-US)

Sponsor contact

CONTACT

+800 00027423 eumedinfo@incyte.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-09