Sign in

NCT07570979RecruitingPhase 1

A Study to Investigate the Safety and Tolerability of Oral INR731 Single Agent or in Combination With Androgen Receptor Pathway Inhibitor (ARPI) in Patients With Metastatic Prostate Cancer

An Open-label, Multi-center, First in Human Phase I Global Dose Escalation and Expansion Study of INR731 Single Agent or in Combination With an Androgen Receptor Pathway Inhibitor in Patients With Metastatic Prostate Cancer

Source: ClinicalTrials.gov · Last updated 23 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to assess the safety, tolerability, pharmacokinetics/pharmacodynamics, preliminary anti-tumor activity, and recommended dose of INR731 as a single agent and in combination with standard-of-care androgen receptor pathway inhibitors (ARPIs) in adult patients with metastatic prostate cancer.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
208 (estimated)
First submitted
30 Apr 2026
Start date
25 May 2026
Primary completion date
3 Jun 2030
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT07570979
EudraCT number
2025-524080-20

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 208
  • From 25 May 2026 to the primary completion date, 3 Jun 2030
  • 12 sites in 8 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients previously treated with a cereblon-based degrader.
  • Treatment with an investigational agent within 7 days (or 5 half-lives, whichever is longer) of the anticipated Cycle 1 Day 1 (C1D1).
    • Other protocol-defined inclusion/exclusion criteria may apply.

Other illness

  • Patients with biochemical recurrence only or those without evidence of metastatic disease by radiographical imaging (CT/MRI or bone scan) are not eligible.
  • Patients who are HIV+ or immune compromised.

Lab values

  • Use of agents known to prolong QT interval unless they can be permanently discontinued for the duration of the study

Age

  • Age \< 18 years old.

Other

  • Histological and/or cytological confirmation of non-adenocarcinoma of the prostate.

Who the study is looking for

  • An Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) ≤2.
  • Participants must have histological and/or cytological confirmation of adenocarcinoma of the prostate. Participants with mixed histology (neuroendocrine) are eligible as long as the non-adenocarcinoma feature is the minority component.
  • At least 1 metastatic lesion (according to local radiology assessment by the investigator) present on baseline CT, MRI, or bone scan imaging obtained ≤28 days prior to Cycle 1 Day 1 (C1D1).
  • Patients must have a castrate level of serum/plasma testosterone (\<50 ng/dL or \<1.7 nmol/L).
  • Ongoing androgen deprivation therapy (ADT) either via orchiectomy and/or ongoing gonadotropin-releasing hormone (GnRH) analog or inhibitor is allowed.
  • Participants must be mCRPC patients who have either progressed on or are not candidates for other SOC. Prior taxane, poly(ADP) ribose polymerase (PARP) inhibitor, and lutetium Lu 177 vipivotide tetraxetan (Pluvicto) are allowed. Combination expansion patients, however, must be 1L mCRPC with no prior treatment in the mCRPC setting. Treatment within the mHSPC setting does not affect eligibility.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis Investigative Site
Coordinator of this site? Confirm its status
MelbourneAustraliaRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
MontrealCanadaRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
DresdenGermanyRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
WürzburgGermanyRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
MadridSpainRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
ValenciaSpainRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
MilanItalyRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
HirakataJapanRecruiting
Novartis Investigative Site
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting
Mass General Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
Mary Crowley Cancer Research
Coordinator of this site? Confirm its status
DallasUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.