No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Male
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
25 (estimated)
Sponsor
Monte Rosa Therapeutics, Inc · Industry
Who this trial is looking for
This trial is looking for men with advanced prostate cancer that has not responded to hormone therapy. If you join, you will take MRT-2359 and apalutamide to see how well this combination works and how safe it is.
Are You a Good Fit for This Trial?
You may be able to join if
I am over 18 years old.
I have been diagnosed with castration-resistant adenocarcinoma of the prostate.
I have not had more than 1 taxane chemotherapy for my cancer.
I am currently undergoing hormone therapy to lower my testosterone.
I have had at least 1 line of treatment with an AR inhibitor.
I can provide a tumor biopsy for testing.
I have a life expectancy of at least 3 months.
I have adequate organ function.
You may not be able to join if
I have had chemotherapy or radiation therapy within the last 21 days.
I have received treatment with a specific type of cancer therapy for GSPT1.
I have had a stem cell transplant and have not fully recovered.
I have received a stem cell transplant in the last 6 months.
I am currently using high doses of steroids.
I have active central nervous system cancer.
I have a history of severe lung inflammation that needed steroids.
I have serious heart problems.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This Phase 2, open-label, multicenter study is conducted in patients with castration-resistant prostate cancer.
Patients in this study receive MRT-2359, an investigational oral medicine, in combination with apalutamide, an oral medicine used to treat prostate cancer. The main purpose of the study is to assess whether this treatment combination can lower prostate-specific antigen (PSA) The study w…
This Phase 2, open-label, multicenter study is conducted in patients with castration-resistant prostate cancer.
Patients in this study receive MRT-2359, an investigational oral medicine, in combination with apalutamide, an oral medicine used to treat prostate cancer. The main purpose of the study is to assess whether this treatment combination can lower prostate-specific antigen (PSA) The study will also evaluate the safety and tolerability of the treatment combination and assess additional measures of anti-tumor activity.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
* Age \> 18 years
* A predicted life expectancy of ≥ 3 months and an ECOG performance status ≤ 1
* Have histologically or cytologically confirmed castration-resistant adenocarcinoma of the prostate without small cell histology and with androgen receptor (AR) mutations
* Have not…
Inclusion Criteria:
* Age \> 18 years
* A predicted life expectancy of ≥ 3 months and an ECOG performance status ≤ 1
* Have histologically or cytologically confirmed castration-resistant adenocarcinoma of the prostate without small cell histology and with androgen receptor (AR) mutations
* Have not had prior treatment with more than 1 prior taxane-based chemotherapy regimen for castration-resistant prostate cancer
* Have no prior treatment with an AR degrader, opevesostat, or similar therapy
* Has ongoing (chemical or surgical) androgen deprivation with serum testosterone \< 50 ng/dL (\< 1.7 nM)
* Has received prior treatment with poly(ADP-ribose) polymerase (PARP) inhibitor, if appropriate, or deemed ineligible to receive treatment by the Investigator, or has refused PARP inhibitor treatment
* Has received prior treatment with at least 1 line of ARPi
* Have disease measurable per Prostate Cancer Working Group 4 (PCWG4) criteria, with or without measurable disease by RECIST 1.1
* Be able to provide a tumor biopsy for biomarker analysis during the Screening period
* Have adequate organ function
Exclusion Criteria:
* • Have received prior chemotherapy, definitive radiation, or biological cancer therapy within 21 days before the first dose of study treatment or have any AEs that have failed to recover to baseline
* Have received prior therapy with a GSPT1 degrader that was discontinued due to an AE
* Have received prior auto-HCT and have not fully recovered from effects of the last transplant
* Have received allogeneic hematopoietic stem cell transplantation within past 6 months and/or have symptoms of graft-versus-host disease
* Current use of chronic systemic steroid therapy in excess of replacement doses
* Have clinically active central nervous system involvement and/or carcinomatous meningitis
* Have a confirmed history of (noninfectious) pneumonitis that required steroids
* Clinically significant cardiac disease
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