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Axelopran and Nivolumab in PD-1-Refractory Metastatic Melanoma (MORALE-MM)

2026年7月9日 更新者:John Kirkwood

A Phase II Trial of MOR Antagonism With Axelopran and Nivolumab in PD-1-Refractory Metastatic Melanoma (MORALE-MM)

This first-in-human study will evaluate the safety, clinical activity, and immunologic effects of combining axelopran with nivolumab in patients with PD-1-refractory unresectable or metastatic cutaneous melanoma. Exploratory analyses incorporating opioid exposure history and post-hoc OPRM1 genotyping will inform future precision immuno-oncology strategies.

調査の概要

状態

まだ募集していません

詳細な説明

Immune checkpoint inhibitors have substantially improved outcomes in melanoma; however, resistance to PD-1 blockade remains a major clinical limitation. Approximately 60% of patients with metastatic melanoma fail to achieve an objective response to anti-PD-1 therapy, and many initial responders ultimately develop acquired resistance. These limitations highlight the need to identify additional, biologically grounded mechanisms of immune escape that can be therapeutically targeted. Importantly, pharmacologic inhibition of MOR with axelopran, a peripherally acting MOR antagonist restores T-cell effector function and enhances antitumor responses to PD-1 inhibition in preclinical oral squamous cell carcinoma models exposed to exogenous opioids. Notably, endogenous μ-opioid signaling in melanoma suppresses antitumor immunity via MOR, providing a rationale for evaluating peripheral MOR antagonism to enhance checkpoint inhibitor efficacy in melanoma. These findings suggest that constitutive MOR signaling may represent a distinct and targetable pathway of immune resistance that has not been addressed in current immunotherapy strategies.

To date, the role of MOR antagonism has not been evaluated clinically in melanoma, and the OPRM1-MOR axis has not been studied as a mechanism of immune escape in humans. This first-in-human study will evaluate the safety, clinical activity, and immunologic effects of combining axelopran with anti-PD-1 therapy in patients with unresectable or metastatic melanoma who have progressed on prior PD-1-based treatment. Post hoc analyses incorporating exogenous opioid exposure and OPRM1 genotype will explore biologically relevant heterogeneity in treatment response and inform future precision-based approaches. Given the strong mechanistic rationale, consistent preclinical evidence of synergy, and the lack of effective options for patients with PD-1-refractory melanoma, this study addresses a critical unmet need and may establish MOR antagonism as a novel therapeutic strategy to overcome immune resistance in melanoma.

研究の種類

介入

入学 (推定)

28

段階

  • フェーズ2
  • フェーズ 1

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:Danielle Bednarz, RN, BSN
  • 電話番号:412-623-1191
  • メール:bednarzdl@upmc.edu

研究連絡先のバックアップ

  • 名前:Amy Rose, RN, BSN
  • 電話番号:412-647-8587
  • メール:kennaj@upmc.edu

研究場所

    • Pennsylvania
      • Pittsburgh、Pennsylvania、アメリカ、15232
        • UPMC Hillman Cancer Center
        • コンタクト:
          • Amy Rose, RN, BSN
          • 電話番号:412-647-8587
          • メール:kennaj@upmc.edu
        • 主任研究者:
          • John M Kirkwood, MD
        • コンタクト:

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:

  1. Histologically confirmed, unresectable or metastatic cutaneous melanoma with documented PD-1-refractory disease, defined as disease progression during or after prior anti-PD-1-based therapy, meeting criteria for either primary or secondary (acquired) resistance, as follows57:

    1. Primary resistance: Disease progression as best response, or stable disease lasting <6 months, following at least 6 weeks (approximately two cycles) of anti-PD-1-based therapy, with progression confirmed by RECIST v1.1.
    2. Secondary (acquired) resistance: Disease progression occurring after an initial objective response (complete or partial response) or durable stable disease (≥6 months) per RECIST v1.1 while receiving anti-PD-1-based therapy, or within 12 weeks of discontinuation of anti-PD-1 therapy following prior clinical benefit.
    3. Note: Disease must have been histologically confirmed through prior pathology assessment conducted as per SOC.
    4. Note: Prior anti-PD-1-based therapy may have been administered as monotherapy or in combination with other agents.
  2. Age ≥ 18 years.
  3. Eastern Cooperative Oncology Group (ECOG) Performance Scale (PS) 0-2
  4. Measurable disease using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.
  5. Patients must have normal organ and marrow function as defined below:

    1. absolute neutrophil count ≥1,000/mcL
    2. platelets ≥75,000/mcL
    3. total bilirubin ≤1.5 × the institutional upper limit of normal (ULN)
    4. AST(SGOT)/ALT(SGPT) ≤2.5 × institutional ULN (≤5 × the institutional ULN for patients with liver metastasis)
    5. Creatinine clearance ≥40 mL/min/1.73 m2 for patients with a creatinine level above institutional normal.
  6. Sexually active fertile subjects and their partners must agree to use highly effective methods of contraception prior to study entry, during the course of the study, and for 5 months after the last dose of treatment (whichever is later). In addition, men must agree not to donate sperm and women must agree not to donate eggs (ova, oocyte) for the purpose of reproduction during these same periods.
  7. Female subjects of childbearing potential must not be pregnant or breastfeeding at screening. Female subjects are considered to be of childbearing potential unless one of the following criteria is met:

    a. Permanent sterilization (hysterectomy, bilateral salpingectomy, or bilateral oophorectomy) or documented postmenopausal status (defined as 12 months of amenorrhea in a woman > 45 years-of-age in the absence of other biological or physiological causes). Note: Documentation may include review of medical records, medical examination, or medical history interview by study site staff.

  8. Ability to understand and the willingness to sign a written informed consent document.
  9. If known to have prior brain metastases, must not have evidence of active (enlarging and/or symptomatic lesions) brain disease on MRI/CT evaluation done within 28 days of start of study treatment.

Exclusion Criteria:

  1. Participant is not a candidate to continue anti-PD-1 therapy due to unresolved toxicities resulting from previous treatment with anti-PD-1 therapy.
  2. Has an active autoimmune disease requiring systemic treatment within the past 3 months, or a syndrome that requires ongoing systemic steroids or immunosuppressive agents. Subjects with vitiligo, Graves' disease, or psoriasis not requiring systemic therapy or resolved childhood asthma/atopy would be an exception to this rule.

    i. Subjects that require intermittent use of bronchodilators or local steroid injections would not be excluded from the study. Subjects with stable hypothyroidism or Sjogren's syndrome will not be excluded from the study.

    ii. Physiological replacement doses of steroids are permitted.

  3. Participant is taking a daily dose of opioids that is >30 morphine milligram equivalents (MME) i. Daily opioid doses ≤30 MME are allowed
  4. Has a history of non-infectious pneumonitis that required steroids, evidence of interstitial lung disease, or currently active non-infectious pneumonitis.
  5. Prior malignancy within 2 years that in the investigator's opinion would be likely to affect the outcomes of the patients with unresectable melanoma.
  6. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
  7. Known HIV or active Hepatitis B or C. Checking viral serology will not be mandated.
  8. Patients with major gastrointestinal surgery within 12 weeks prior to the first dose of study treatment. Patients who have a colostomy will be excluded from the trial.
  9. Are unable to swallow pills or have known active inflammatory gastrointestinal disease, chronic diarrhea, previous gastric resection or lap band dysphagia, short-gut syndrome, gastroparesis, or other condition that limits the ingestion or gastrointestinal absorption of drugs administered orally.

    i. Note: Gastroesophageal reflux disease under medical treatment is allowed (assuming no drug interaction potential).

  10. Subjects taking moderate to strong CYP3A inhibitors or P-gp inhibitors

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:Axelopran + Nivolumab

Run in (1 week):

Days -6 to 0, Axelopran monotherapy with dose escalating to 15mg PO daily by day 0

Combination Phase:

Axelopran: 15 mg PO daily Nivolumab: 480 mg IV q4w (until disease progression, up to 3 years)

A peripherally restricted mu-opioid receptor antagonist (PAMORA) designed to mitigate the undesirable peripheral effects of opioids without compromising their central analgesic action.
他の名前:
  • VOQUEZNA®
An immune checkpoint inhibitor that helps the immune system attack cancer cells by blocking PD-1 receptors.
他の名前:
  • OPDIVO Qvantig

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
Adverse Events Related to Treatment
時間枠:Up to 30 days post end of treatment
Adverse events (AEs), serious adverse events (SAEs), AEs leading to discontinuation or death, and severity of AEs as assessed by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5.0) determined to be possibly, probably or definitely related to study treatment.
Up to 30 days post end of treatment
Best objective response rate (BORR)
時間枠:Up to 3 years
The proportion of subjects with a confirmed best objective response of Complete Response (CR) or Partial Response (PR) based on RECIST v1.1. CR: Disappearance of all target lesions. Pathological lymph nodes must decrease to a short axis of < 10 mm. All non-target lesions must have disappeared, and tumor markers must have normalized. PR: At least a 30% decrease in the sum of diameters of target lesions, using baseline measurements as a reference.
Up to 3 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Duration of response (DOR)
時間枠:Up to 3 years
Time from date of first documented response Complete Response (CR) or Partial Response (PR) to date of documented Progressive Disease (PD) or death from any cause, based on RECIST v1.1. CR: Disappearance of all target lesions. Pathological lymph nodes must decrease to a short axis of < 10 mm. All non-target lesions must have disappeared, and tumor markers must have normalized. PR: At least a 30% decrease in the sum of diameters of target lesions, using baseline measurements as a reference. PD: At least 20% increase in the sum of diameters of target lesions, taking the smallest sum on study (nadir) as the reference. In addition to the 20% relative increase, the sum must also show an absolute increase of at least 5 mm. The unequivocal progression of non-target lesions or the appearance of any new lesion also classifies as PD.
Up to 3 years
Best Treatment Response in Target lesions
時間枠:Up to 3 years
Best treatment response in target lesions based on RECIST v1.1. CR: Disappearance of all target lesions. Pathological lymph nodes must decrease to a short axis of < 10 mm. All non-target lesions must have disappeared, and tumor markers must have normalized. PR: At least a 30% decrease in the sum of diameters of target lesions, using baseline measurements as a reference.
Up to 3 years
Progression-free Survival (PFS)
時間枠:Up to 3 years
Time from date of first dose of study treatment to date of first documented Progressive Disease (PD) based on RECIST v1.1, or death from any cause, whichever occurs first. PD: At least 20% increase in the sum of diameters of target lesions, taking the smallest sum on study (nadir) as the reference. In addition to the 20% relative increase, the sum must also show an absolute increase of at least 5 mm. The unequivocal progression of non-target lesions or the appearance of any new lesion also classifies as PD. iUPD (Unconfirmed Progressive Disease) requires a follow-up scan to confirm whether it is true tumor growth or temporary.
Up to 3 years
Overall survival (OS)
時間枠:Up to 4.5 years
Overall survival, defined as the time from date of first dose of study treatment to date of death from any cause.
Up to 4.5 years
Immune best objective response rate (iBORR)
時間枠:Up to 3 years
Proportion of subjects with a confirmed best objective response to immunotherapy of CR or PR based on iRECIST . CR: Disappearance of all target lesions. Pathological lymph nodes must decrease to a short axis of < 10 mm. All non-target lesions must have disappeared, and tumor markers must have normalized. PR: At least a 30% decrease in the sum of diameters of target lesions, using baseline measurements as a reference. CR or PR iUPD (one or more instances), but not iCPD, before iCR, iPR.
Up to 3 years
Immune duration of response (iDOR)
時間枠:Up to 3 years
Time from date of first documented response (CR or PR) to date of documented PD or death from any cause, based on iRECIST. CR: Disappearance of all target lesions. Pathological lymph nodes must decrease to a short axis of < 10 mm. All non-target lesions must have disappeared, and tumor markers must have normalized. PR: At least a 30% decrease in the sum of diameters of target lesions, using baseline measurements as a reference. CR or PR iUPD (one or more instances), but not iCPD, before iCR, iPR.
Up to 3 years
Immune progression-free survival (iPFS)
時間枠:Up to 3 years
Time from date of first dose of study treatment to date of first documented PD based on iRECIST, or death from any cause, whichever occurs first. PD: At least 20% increase in the sum of diameters of target lesions, taking the smallest sum on study (nadir) as the reference. In addition to the 20% relative increase, the sum must also show an absolute increase of at least 5 mm. The unequivocal progression of non-target lesions or the appearance of any new lesion also classifies as PD. iUPD (Unconfirmed Progressive Disease) requires a follow-up scan to confirm whether it is true tumor growth or temporary.
Up to 3 years

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。

スポンサー

協力者

捜査官

  • 主任研究者:John M Kirkwood, MD、UPMC Hillman 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10月31日

一次修了 (推定)

2028年7月31日

研究の完了 (推定)

2030年7月31日

試験登録日

最初に提出

2026年5月29日

QC基準を満たした最初の提出物

2026年5月29日

最初の投稿 (実際)

2026年6月8日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月13日

QC基準を満たした最後の更新が送信されました

2026年7月9日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

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?

いいえ

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はい

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いいえ

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