A Study of Mevrometostat With Enzalutamide in People With Prostate Cancer Who Have Previously Received Androgen Receptor Pathway Inhibitor Therapy (MOMENT)
2026年5月11日 更新者:Prostate Cancer Clinical Trials Consortium
A Phase 2, Open-label, Single-Arm Study of Mevrometostat Plus Enzalutamide in Metastatic Castration-Resistant Prostate Cancer Following Prior Androgen Receptor Pathway Inhibitor Therapy (MOMENT)
The purpose of this study is to find out whether mevrometostat in combination with enzalutamide delays cancer progression in people with metastatic castration-resistant prostate cancer (mCRPC) who have previously received enzalutamide, darolutamide, or apalutamide in the metastatic castration-sensitive prostate cancer (mCSPC) or non-metastatic castration-resistant prostate cancer (nmCRPC) setting but have not previously progressed on abiraterone.
調査の概要
研究の種類
介入
入学 (推定)
60
段階
- フェーズ2
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Sarah Wise
- 電話番号:215-380-9051
- メール:wises@mskcc.org
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
Inclusion Criteria:
- Willing and able to provide written informed consent
- Age 18 years or older
- Diagnosis of prostate cancer (adenocarcinoma) confirmed by tissue sample, without neuroendocrine or small cell features
- Currently taking or recently treated with enzalutamide, darolutamide, or apalutamide (within 30 days of screening) and willing to switch to or restart enzalutamide for this study
- Cancer has spread to bone or soft tissue (metastatic disease), confirmed by imaging
- ECOG performance status of 0, 1, or 2 (able to care for self and up and about more than 50% of waking hours)
- Testosterone level less than 50 ng/dL at screening, with ongoing hormone deprivation therapy or prior surgical castration
- If receiving bone-protective therapy (e.g., denosumab or bisphosphonates), must be on a stable dose for at least 4 weeks
- Evidence of cancer progression while on enzalutamide, darolutamide, or apalutamide, shown by rising PSA, worsening disease on imaging, or new bone lesions
- Adequate organ function based on blood tests within 28 days of starting treatment, including adequate blood counts, kidney function, and liver function
- Willing to use acceptable birth control during the study and for 30 days after the last dose
Exclusion Criteria:
- History of myelodysplastic syndrome, acute myeloid leukemia, or other prior cancer (exceptions: non-melanoma skin cancer, carcinoma in situ, cancers more than 3 years ago with no recurrence, or early-stage cancers with low risk of recurrence)
- Any medical or psychiatric condition, including active infection or recent suicidal ideation, that may make study participation unsafe
- History of seizure or conditions that may increase seizure risk (e.g., prior stroke, significant brain trauma), or loss of consciousness or transient ischemic attack within 12 months
- Untreated brain metastases, spinal cord compression, or clinically significant epidural disease
- Use of 5-alpha reductase inhibitors, herbal medications, or supplements known to alter PSA levels within 4 weeks of starting treatment
- AIDS-related illness or active hepatitis B or C (well-controlled HIV is allowed)
- Known history of chronic liver disease (e.g., alcoholic liver disease, primary biliary cirrhosis, autoimmune hepatitis, Wilson's disease, hemochromatosis)
- Known history of active inflammatory gastrointestinal disease, chronic diarrhea, or prior gastric resection or lap-band surgery
- Clinically significant cardiovascular disease within the past 6 months (e.g., heart attack, unstable angina, stroke, heart failure NYHA Class III/IV, pulmonary embolism, significant arrhythmias), cardiac pacemaker, or QTcF greater than 480 msec on screening ECG
- Prior or current use of PARP inhibitors and/or AKT inhibitors
- Prior cancer progression on abiraterone (stopping abiraterone due to side effects is allowed)
- Known allergy to any study drug
- Blood transfusion within 28 days prior to screening blood tests
- Use of another investigational drug within 4 weeks before starting study treatment
- Any other condition that, in the opinion of the investigator, would prevent safe participation
- Current use or anticipated need for strong CYP3A4/5 inhibitors or inducers (other than enzalutamide) within 10 days or 5 half-lives prior to treatment start
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Mevrometostat + Enzalutamide
Mevrometostat 875 mg orally twice daily (BID) with food in combination with enzalutamide 160 mg orally once daily.
Treatment continues until confirmed radiographic disease progression, unacceptable toxicity, or other protocol-defined discontinuation criteria.
|
875 mg oral tablet, taken twice daily with food
他の名前:
160 mg oral capsule, taken once daily
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Radiographic progression free survival (rPFS)
時間枠:From treatment initiation until documented disease progression, death, lost to follow-up, withdrawal, administrative censoring at the time of final analysis, whichever comes first, assessed up to 24 months.
|
rPFS by RECIST v1.1 and PCWG3 defined as time from start of study treatment to the earlier of first documentation of objective progressive disease by RECIST v1.1 or PCWG3 or death due to any cause.
|
From treatment initiation until documented disease progression, death, lost to follow-up, withdrawal, administrative censoring at the time of final analysis, whichever comes first, assessed up to 24 months.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall Survival (OS)
時間枠:From start of study treatment until death from any cause, assessed up to 24 months.
|
Overall survival as determined by survival status during study participation.
OS is defined as the time from the start of study treatment to the date of death due to any cause.
|
From start of study treatment until death from any cause, assessed up to 24 months.
|
|
Proportion of Participants Achieving 50% Decline in PSA (PSA50 Response)
時間枠:From initiation of study treatment through study completion, assessed up to 24 months.
|
Proportion of participants with detectable PSA values at baseline with a 50% decline in PSA confirmed by a subsequent PSA value obtained ≥3 weeks later.
|
From initiation of study treatment through study completion, assessed up to 24 months.
|
|
Time to PSA Progression as Defined by PCWG3
時間枠:From start of study treatment until documented PSA progression, assessed up to 24 months.
|
Time from first dose of mevrometostat to the date of a ≥25% increase in PSA over nadir with an absolute increase of ≥2 ng/mL, confirmed by a second consecutive PSA value at ≥3 weeks later.
|
From start of study treatment until documented PSA progression, assessed up to 24 months.
|
|
Number of Participants with Treatment-Related Adverse Events as Assessed by CTCAE v5.0
時間枠:From start of study treatment through 28 days after last dose of study drug, assessed up to 24 months.
|
Incidence of adverse events characterized by type, severity according to CTCAE version 5.0, timing, seriousness, and relationship to study treatment.
|
From start of study treatment through 28 days after last dose of study drug, assessed up to 24 months.
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
捜査官
- 主任研究者:Atish Choudhury, MD, PhD、Dana-Farber Cancer Institute
- 主任研究者:Michael Schweizer, MD、University of Washington- Fred Hutch Cancer Center
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年8月1日
一次修了 (推定)
2029年5月1日
研究の完了 (推定)
2029年8月1日
試験登録日
最初に提出
2026年5月4日
QC基準を満たした最初の提出物
2026年5月11日
最初の投稿 (実際)
2026年5月18日
学習記録の更新
投稿された最後の更新 (実際)
2026年5月18日
QC基準を満たした最後の更新が送信されました
2026年5月11日
最終確認日
2026年5月1日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- c25-392
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
はい
IPD プランの説明
The Prostate Cancer Clinical Trials Consortium, LLC supports the international committee of medical journal editors (ICMJE) and the ethical obligation of responsible sharing of data from clinical trials.
The protocol summary, a statistical summary, and informed consent form will be made available on clinicaltrials.gov
when required as a condition of Federal awards, other agreements supporting the research and/or as otherwise required.
Requests for deidentified individual participant data can be made beginning 12 months after publication and for up to 36 months post publication.
Deidentified individual participant data reported in the manuscript will be shared under the terms of a Data Use Agreement and may only be used for approved proposals.
Requests may be made to: pcctc@mskcc.org.
IPD 共有サポート情報タイプ
- ICF
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
はい
米国FDA規制機器製品の研究
いいえ
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