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Phase 1/2 Study of Intravenous Injection of STX-003 in Advanced Solid Tumors as Monotherapy or in Combination With Pembrolizumab

2026年8月3日 更新者:Strand Therapeutics Inc.

A Phase 1/2, Open-label, Multi-center, First-in-human Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Antitumor Activity of STX-003 Delivered Intravenously in Patients With Advanced Solid Tumors as a Monotherapy or in Combination With Pembrolizumab

Phase 1/2, Open-label, Multi-center, First-in-human Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Anti-tumor Activity of STX-003 Delivered by Intravenous Injection in Patients with Advanced Solid Tumors as a Monotherapy or in Combination with Pembrolizumab.

調査の概要

詳細な説明

This open-label, Phase 1/2, first-in-human (FIH), multiple ascending dose and dose expansion study involves STX-003 administration, alone or in combination with pembrolizumab, to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity in patients with advanced cancers. (Update after review)

研究の種類

介入

入学 (推定)

220

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

研究場所

    • Arizona
      • Scottsdale、Arizona、アメリカ、85258
        • 募集
        • HonorHealth Research Institute
        • 主任研究者:
          • Justin Moser, MD
        • コンタクト:
    • Tennessee
      • Nashville、Tennessee、アメリカ、37203
        • 募集
        • Sarah Cannon Research Institute
        • 主任研究者:
          • Melissa Johnson, 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:

  • Inclusion Criteria (Phase 1 and Phase 2)

    1. Mentally competent and able to understand and sign the ICF.
    2. Tumor type for which there is an FDA-approved anti-PD-1/L1 antibody therapy, specifically including biomarker labeled subsets (i.e. PD-L1+) as well as anatomical subsets in some disease (cutaneous melanoma is eligible whereas acral, mucosal and uveal are not; Phase 1) and advanced cutaneous melanoma or PD-L1+ NSCLC.
    3. Histologically or cytologically documented, locally advanced, or metastatic solid tumor.
    4. At least one measurable lesion per RECIST v1.1 criteria.
    5. The patient lacks a curative therapy or has progressive disease despite, or refused, standard therapy.
    6. ECOG performance status of 0 or 1.
    7. Life expectancy of ≥ 12 weeks per the Investigator.
    8. ≥ 18 years of age at the time of informed consent.
    9. Body weight ≥ 40 kg.
    10. WOCBP and males with female partners of child-bearing potential must agree to use adequate birth control throughout their participation and for 3 months following the last dose of STX-003.
    11. Willing and able to comply with protocol required assessments.

Hematology:

  • ANC ≥ 1,000 cells/mm3.
  • Platelet count ≥ 75,000 cells/mm3.
  • Hemoglobin ≥ 8.0 g/dL.

    • Renal: Serum creatinine < 1.5 × ULN or creatinine clearance ≥ 40 mL/min based on the Cockcroft-Gault glomerular filtration rate estimation

Coagulation:

  • PT/INR or PT must be ≤ 1.5 × ULN.
  • aPTT ≤ 1.5 × ULN unless undergoing anticoagulation therapy.

    • Liver:

  • Albumin ≥ 3.5 g/dL or within the normal range of the local reference laboratory.
  • AST and ALT < 2 × ULN.
  • Bilirubin ≤ 1.5 × ULN (except participants with documented Gilbert's syndrome who may be enrolled if the conjugated bilirubin is within normal limits) or ≤ 5 × ULN with liver metastases.

Phase 2 Inclusion Criteria

13. NSCLC :

  • Histologically or cytologically documented findings consistent with NSCLC not amenable to curative surgery, radiation, or other therapy.
  • Biomarker confirmed as PD-L1+ per local institutional standard practice.
  • Patients with known activating EGFR, STK11 or KEAP1 mutations as well as ALK/ROS1 fusions, are not eligible.
  • Prior treatment (for advanced, metastatic or [neo]adjuvant) should have included a platinum-based therapy and a PD-1/L1 pathway checkpoint inhibitor, unless the patient is not a candidate for or has refused viable therapies due to inability to tolerate treatment (i.e. cell therapy) or potential side effects (i.e. checkpoint inhibitor toxicity).

    14. Melanoma : Histologically or cytologically documented findings consistent with advanced cutaneous melanoma not amenable to curative surgery, radiation, or other therapy. Acral, mucosal and uveal melanoma are excluded.

  • Patients who are not candidates for or have refused available therapies due to inability to tolerate treatment (i.e. cell therapy) or potential side effects (i.e. checkpoint inhibitor toxicity) are also eligible.
  • Received an anti-PD-1/PD-L1 inhibitor as monotherapy or in combination with anti-CTLA-4 inhibitor and have either primary or secondary checkpoint inhibitor resistance asper SITC consensus definition, unless deemed intolerable by the Investigator. Patients with BRAF V600E mutant melanoma should have received a BRAF inhibitor as monotherapy or in combination with other targeted agents (MAPK kinase MEK inhibitors), unless deemed intolerable by the Investigator.

Exclusion Criteria:

  • Exclusion Criteria (Phase 1 and 2)

    1. Medical Conditions

      • History of primary immune deficiency.
      • History of clinically significant autoimmune disease that has required intervention in the last 6 months. Consultation with the MM may inform the discussion of whether autoimmune disease is clinically significant.
      • History of Grade 3 or higher IRAEs that has not resolved to Grade ≤ 1 at the time of enrollment. Exceptions include endocrine disorders that are well-managed with stable physiological hormone replacement and Grade 3 immune-related rash. Patients meeting this criterion may be considered for enrollment following approval by the MM.
      • History of solid organ transplant and taking immunosuppressive medications.
    2. Cardiovascular exclusions

      • Medical history of an arterial thrombotic event, stroke, or transient ischemic attack within the past 6 months.
      • Medical history of symptomatic congestive heart failure (New York Heart Association classes II-IV) or a cardiac arrhythmia that required treatment within the past 6 months.
      • Medical history of myocardial infarction or unstable angina within 6 months before C1D1.
    3. Recent medical concerns exclusions

      • Evidence of active infection requiring IV antibiotics within 7 days prior to C1D1.
      • Active uncontrolled bleeding, or a bleeding diathesis within 7 days prior to C1D1.
      • Serious or non-healing wound, fistula, skin ulcer, or non-healing bone fracture within 7 days prior to C1D1.
      • Known HIV infection, active hepatitis B infection, or hepatitis C infection:
  • Virology evaluation should be conducted at Screening to include serum HIV antibody, HBc antibody, HBsAg antigen, and HCV antibody. Patients with a positive antibody evaluation for HCV and/or HBc should undergo evaluation to measure HCV RNA or HBV DNA, respectively.

    • Untreated CNS tumor, epidural tumor or metastasis, or brain metastasis. Patients with any primary CNS malignancy including glioma and current, active, or progressing CNS malignancy, including carcinomatosis meningitis, are excluded.
    • Patients with treated brain metastases are eligible if there is no evidence of progression for at least 4 weeks after CNS-directed treatment, as ascertained by clinical examination and brain imaging (MRI or CT scan) during the Screening period and are off systemic steroids (for at least 2 weeks prior to first dose).
    • Another primary malignancy that has not been treated with curative intent (discuss with MM), except for non-metastatic cutaneous basal cell or squamous cell carcinoma, or non-muscle invasive bladder cancer.
    • Serious illness considered by the Investigator as incompatible with participating in this clinical study.
    • Major surgery within 4 weeks of first dose of study drug.
    • Any condition that, in the opinion of the Investigator, would interfere with evaluation of the investigational product or interpretation of the patients' safety or study results.

      4. Prior/Concomitant Therapy

    • Prior treatment with STX-003 or other VEEV-based replicating RNA.
    • Prior IL-12 therapy.
    • Receipt of any live vaccine within 30 days prior to the first dose of study treatment.
    • Use of another systemic anticancer therapy within 3 weeks prior to C1D1 or 5 halflives, whichever is shorter or use of radiotherapy within 1 week prior to C1D1 5. Prior/Concurrent Clinical Study Experience
    • Previously enrolled in this study.
    • Actively enrolled in another clinical study unless it is an observational (noninterventional) clinical study or the follow-up component of an interventional study.
    • Known severe hypersensitivity (Grade ≥ 3) to study treatment or any of the excipients of the products.

Other Exclusions

  • History of interstitial lung disease or active, non-infectious pneumonitis (combination cohorts only).
  • Known psychiatric or substance use disorder that would interfere with the patient's ability to cooperate with the requirements of the study.
  • Currently pregnant (confirmed with a positive pregnancy test), breast-feeding or planning to become pregnant within 6 months following treatment. For WOCBP, a negative serum β-HCG result must be available within a 72-hour window before the first treatment dose.

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:非ランダム化
  • 介入モデル:並列代入
  • 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:Phase 1 Monotherapy
STX-003 administered intravenously, at ascending doses across sequential cohorts, once per cycle for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
実験的:Phase 1 Combination (STX-003 with Pembrolizumab)
STX-003 administered intravenously, at ascending doses across sequential cohorts, once per cycle in combination with pembrolizumab for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
Pembrolizumab (Keytruda USPI 2026) is a marketed PD-1 blocking humanized monoclonal IgG4 kappa antibody.
実験的:Phase 2 Monotherapy (STX-003)
STX-003 administered intravenously, at 4 planned dose expansion cohorts in patients with advanced cancers with high unmet need, once per cycle for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
実験的:Phase 2 Combination (STX-003 with Pembrolizumab)
STX-003 administered intravenously, at 4 planned dose expansion cohorts in patients with advanced cancers with high unmet need, once per cycle for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
Pembrolizumab (Keytruda USPI 2026) is a marketed PD-1 blocking humanized monoclonal IgG4 kappa antibody.

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
Incidence of TEAEs, SAEs, and DLTs
時間枠:From time of informed consent until 30 days after the last dose of investigational product.
From time of informed consent until 30 days after the last dose of investigational product.
Occurrence of changes from baseline in patients' clinical safety laboratory values and vital signs to assess the safety and tolerability of STX-003.
時間枠:From Day 1 until 30 days after last dose of STX-003
Collection and analysis of changes in data from baseline of patients' safety laboratory values (chemistry, hematology, coagulation, complement (Bb & C3a), urinalysis, and lipids). Vital signs will include Temperature: (degrees Fahrenheit) Pulse: (beats per minute) Respiratory rate: (breaths per minute) Blood pressure: (systolic and diastolic each reported in mmHg) Oxygen saturation by pulse oximetry: (percentage (SpO2, %))
From Day 1 until 30 days after last dose of STX-003

二次結果の測定

結果測定
メジャーの説明
時間枠
Assessment of PK and PD in patients dosed with STX-003
時間枠:Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Area under the concentration curve (AUC)
Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Number and nature of preliminary antitumor activity of STX-003 as monotherapy and in combination with Pembrolizumab.
時間枠:From time of informed consent until 30 days after the last dose of investigational product.
From time of informed consent until 30 days after the last dose of investigational product.
Assessment of Tumor infiltrating lymphocytes
時間枠:From time if informed consent until 30 days after the last dose of investigational product (STX-003)
Tumor biopsies will be analyzed by immunohistochemistry to assess tumor-infiltrating lymphocytes (TILs) in the tumor microenvironment, including density of CD4 and CD8 positive cells and PD-L1 expression.
From time if informed consent until 30 days after the last dose of investigational product (STX-003)
Objective Response Rate (ORR) in patients with advanced solid tumors.
時間枠:From time of informed consent until 30 days after the last dose of investigational product.
From time of informed consent until 30 days after the last dose of investigational product.
Assessment of PK and PD in patients dosed with STX-003
時間枠:Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Maximum observed plasma concentration (Cmax) of STX-003
Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Changes from baseline in vital signs
時間枠:From Day 1 until 30 days after last dose of STX-003.
Vital signs will include Temperature: (degrees Fahrenheit) Pulse: (beats per minute) Respiratory rate: (breaths per minute) Blood pressure: (systolic and diastolic each reported in mmHg) Oxygen saturation by pulse oximetry: (percentage (SpO2, %))
From Day 1 until 30 days after last dose of STX-003.

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

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 (実際)

2026年6月30日

一次修了 (推定)

2030年7月17日

研究の完了 (推定)

2030年11月15日

試験登録日

最初に提出

2026年4月6日

QC基準を満たした最初の提出物

2026年8月3日

最初の投稿 (実際)

2026年8月6日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月6日

QC基準を満たした最後の更新が送信されました

2026年8月3日

最終確認日

2026年8月1日

詳しくは

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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

米国FDA規制機器製品の研究

いいえ

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