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ALT-100 Monoclonal Antibody (mAb) in Bone-Predominant Metastatic Androgen Pathway Modulation Resistant (APMR) Prostate Cancer -- The ALTAR-100 Trial

2026年11月3日 更新者:University of Florida

Aqualung Therapeutics Corporation has developed ALT-100, a humanized murine monoclonal antibody (mAb) that specifically targets and neutralizes extracellular nicotinamide phosphoribosyltransferase (eNAMPT) and prevents activation of a dysregulated proinflammatory signaling cascade.

Pre-clinical and clinical information from acute respiratory distress syndrome and prostate cancer studies show a novel treatment option for the patients with androgen pathway modulator-resistant (APMR) prostate cancer and bone metastases. Secreted eNAMPT drives prostate cancer progression, and a humanized eNAMPT-neutralizing antibody prevented aggressive disease in preclinical models by Sun et al. The anti-fibrotic activity of the eNAMPT-neutralizing antibody acts on type I collagen turnover-the same biology as osteoblastic bone metastasis.

Bone-predominant androgen pathway modulator-resistant (APMR) prostate cancer is a common clinical problem. Treatment options are often limited after progression on ADT and androgen receptor pathway inhibitors. The bone microenvironment itself is still largely untargeted. No eNAMPT-directed therapy has been tested in any oncology population, and no trial has asked whether eNAMPT/toll-like receptor 4 (TLR4) blockade can modify the osseous tumor microenvironment in humans. This trial would test a first-in-class agent aimed at the bone microenvironment rather than at the tumor alone, in a setting where most available therapies offer short-lived benefit.

This study will evaluate the safety, tolerability and efficacy of the use of ALT-100 for treatment of bone-predominant metastatic androgen pathway modulation resistant prostate cancer. The recommended phase 2 dose of ALT-100 for treatment of bone-predominant metastatic androgen pathway modulation resistant prostate cancer will also be determined in the phase 1 portion of this study.

調査の概要

状態

まだ募集していません

介入・治療

研究の種類

介入

入学 (推定)

42

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:Alexandra Leggett
  • 電話番号:352-273-9785
  • メール:agmueller@ufl.edu

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

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

男

説明

Inclusion Criteria:

  • Male, age ≥ 18 years

  • Prostate cancer, histologically confirmed or presumed on the basis of clinical, biochemical, and/or radiographic findings.

  • Metastatic disease confined to bone and lymph nodes, with bone metastases predominant, documented on conventional imaging (CT/MRI and bone scan). Measurable soft tissue disease is not required.

  • Androgen pathway modulation-resistant (APMR) disease per Prostate Cancer Working Group 4 (PCWG4) with progression on at least one prior androgen receptor pathway inhibitor documented as any of the following:

    1. Serum PSA progression defined as 2 consecutive increases in PSA over a previous reference value measured at least 1 week prior. The minimal start value is 2.0 ng/mL,
    2. Soft tissue progression defined as an increase ≥20% in the sum of the diameter (SOD) (short axis for nodal lesions and long axis for non-nodal lesions) of all target lesions based on the smallest SOD since treatment started or the appearance of one or more new lesions or unequivocal progression of existing non-target lesions,
    3. For PSMA-PET: Two new PSMA-avid lesions, or
    4. Progression of bone disease defined by the appearance of ≥2 new bone lesions on bone scan per PCWG4 criteria
  • Ongoing androgen deprivation therapy (ADT) with a Gonadotropin-releasing hormone analogue, or prior bilateral orchiectomy, with serum testosterone <50 ng/dL

  • ECOG performance status 0-2

  • Life expectancy ≥6 months

  • Adequate organ and marrow function defined as:

    1. ANC ≥1,500/µL
    2. Platelets ≥100,00/µL
    3. Hemoglobin ≥9.0 g/dL without transfusion within 14 days
    4. Total bilirubin ≤1.5 x ULN (≤ 3 x ULN for Gilbert's)
    5. AST and ALT ≤3 x ULN
    6. Creatinine clearance ≥30 mL/min
  • Concurrent bone-modifying agent (including, but not limited to denosumab or bisphosphonates such as zoledronic acid or pamidronate), permitted but not required. If receiving one, it must have been at a stable dose and scheduled for ≥8 weeks before C1D1.

  • Written informed consent obtained from the subject and the subject agrees to comply with all the study-related procedures.

  • Subjects with partners of child-bearing potential must agree to use physician-approved contraceptive methods (e.g., abstinence, condoms, vasectomy) throughout the study and should avoid conceiving children for 6 months following the last dose of study drug.

Exclusion Criteria:

  • Visceral metastases, including liver, lung, adrenal, brain or peritoneal disease. Lymph node involvement is permitted
  • Known pure small cell or neuroendocrine prostate carcinoma
  • Radium-223 within 6 months of C1D1
  • External beam radiotherapy to a bone lesion within 4 weeks of C1D1 or radiotherapy planned during the DLT window of 30 days after first dose of ALT-100.
  • Impending skeletal-related event requiring immediate radiotherapy or surgical intervention or untreated spinal cord compression
  • Chemotherapy, investigational therapy, or any systemic anticancer therapy other than ADT within 4 weeks or 5 half-lives of C1D1, whichever is shorter
  • Prior exposure to any extracellular nicotinamide phosphoribosyltransferase (eNAMPT)-directed or toll-like receptor 4 (TLR4)-directed therapeutic agent.
  • Known hypersensitivity to a monoclonal antibody, or prior grade ≥3 infusion-related reaction to a biologic
  • Active infection requiring systemic therapy at C1D1
  • Known HIV infection, or known active hepatitis B or hepatitis C, that is uncontrolled or requires a change in therapy. Testing is not required at screening
  • Cardiovascular or thromboembolic disease that, in the investigator's judgment, is uncontrolled or would place the patient at undue risk on study
  • Chronic systemic immunosuppressive therapy at doses that in the investigator's judgement would place the patient at undue infection risk
  • Active osteonecrosis of the jaw, or invasive dental procedure planned during the DLT window of 30 days after first dose of ALT-100
  • Another malignancy requiring active treatment, except non-melanoma skin cancer or adequately treated in situ disease
  • Any condition that in the investigator's judgement would compromise safety or protocol compliance
  • Administration of a vaccine containing live virus within 30 days prior to the first dose of trial treatment. Note: Most flu vaccines are killed viruses, with the exception of the intra-nasal vainer (Flu-Mist) which is an attenuated live virus and therefore prohibited for 30 days prior to first dose.
  • Prisoners or subjects who are involuntarily incarcerated, or subjects who are compulsorily detained for treatment of either a psychiatric or physical illness.

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:ランダム化
  • 介入モデル:順次割り当て
  • 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:Phase 1 - Dose level 1 - 1.0 mg/kg ALT-100

This is the starting dose for the phase 1 portion of the study.

Participants will receive either 1.0 mg/kg or 4.0 mg/kg of ALT-100 intravenously once every 28 days for up to 6 treatment cycles while receiving standard of care androgen deprivation therapy. The assigned dose will determined by either a 3 + 3 design (for phase 1) or 1:1 randomization (for phase 2).

実験的:Phase 1 - Dose Level 2 - 4.0 mg/kg of ALT-100

This is the second dose level that will be tested in the phase 1 portion of the study.

Participants will receive either 1.0 mg/kg or 4.0 mg/kg of ALT-100 intravenously once every 28 days for up to 6 treatment cycles while receiving standard of care androgen deprivation therapy. The assigned dose will determined by either a 3 + 3 design (for phase 1) or 1:1 randomization (for phase 2).

実験的:Phase 2 - Recommended phase 2 dose of ALT-100

Participants randomized to this arm will receive the recommended phase 2 dose determined in the phase 1 portion of the study.

Participants will receive either 1.0 mg/kg or 4.0 mg/kg of ALT-100 intravenously once every 28 days for up to 6 treatment cycles while receiving standard of care androgen deprivation therapy. The assigned dose will determined by either a 3 + 3 design (for phase 1) or 1:1 randomization (for phase 2).

アクティブコンパレータ:Phase 2 - Comparator dose of ALT-100

Participants randomized to this arm will receive a comparator dose of ALT-100 that is not the recommended phase 2 dose determined in phase 1.

Participants will receive either 1.0 mg/kg or 4.0 mg/kg of ALT-100 intravenously once every 28 days for up to 6 treatment cycles while receiving standard of care androgen deprivation therapy. The assigned dose will determined by either a 3 + 3 design (for phase 1) or 1:1 randomization (for phase 2).

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 dose limiting toxicities
時間枠:first 30 days of treatment with ALT-100

Determine the incidence of dose-limiting toxicities during the dose-limiting toxicity evaluation period for participants on the phase 1 portion.

first 30 days of treatment with ALT-100
Percentage of participants who achieve a PSA decrease of at least 30%
時間枠:After up to 6 months of treatment with ALT-100

Compare the percentage of participants on each arm on the phase 2 portion who achieve a PSA decrease of at least 30%

After up to 6 months of treatment with ALT-100
Percentage of participants who achieve a PSA decrease of at least 50%
時間枠:After up to 6 months of treatment with ALT-100

Compare the percentage of participants on each arm on the phase 2 portion who achieve a PSA decrease of at least 50%

After up to 6 months of treatment with ALT-100
Radiographic progression-free survival
時間枠:After up to 6 months of treatment with ALT-100

Compare the radiographic progression-free survival (per Prostate Cancer Working Group 4) of participants on each arm on the phase 2 portion.

After up to 6 months of treatment with ALT-100

二次結果の測定

結果測定
メジャーの説明
時間枠
Maximum plasma concentration of ALT-100
時間枠:At 4 hours after each dose of ALT-100

Determine the maximum plasma concentration of ALT-100 for participants on the Phase 2 portion.

At 4 hours after each dose of ALT-100
Time to reach maximum plasma concentration of ALT-100
時間枠:At 4 hours after each dose of ALT-100

Determine the time to reach maximum plasma concentration of ALT-100 for participants on the Phase 2 portion.

At 4 hours after each dose of ALT-100
Area under the curve (AUC) up to the last measurable plasma concentration for ALT-100
時間枠:At 4 hours after each dose of ALT-100

Determine the area under the curve (AUC) up to the last measurable plasma concentration for ALT-100 for participants on the Phase 2 portion.

At 4 hours after each dose of ALT-100
Area under the curve (AUC) over the dosing interval for ALT-100
時間枠:Over the 4 weeks between doses of ALT-100

Determine the area under the curve (AUC) over the dosing interval for ALT-100 for participants on the Phase 2 portion.

Over the 4 weeks between doses of ALT-100
Half-life for ALT-100
時間枠:At 4 hours after each dose of ALT-100

Determine the half-life for ALT-100 for participants on the Phase 2 portion.

At 4 hours after each dose of ALT-100
Trough plasma concentration for ALT-100
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Determine the trough plasma concentration for ALT-100 for participants on the Phase 2 portion.

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Average plasma concentration during a dosing interval for ALT-100
時間枠:Over the 4 weeks between doses of ALT-100

Determine the average plasma concentration during a dosing interval for ALT-100 for participants on the Phase 2 portion.

Over the 4 weeks between doses of ALT-100
Plasma concentration of eNAMPT
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of eNAMPT

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of IL-6
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of IL-6

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of IL-8
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of IL-8

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of TNF-a
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of TNF-a

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of IL-1b
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of IL-1b

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of IL-1RA
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of IL-1RA

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of Ang2
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of Ang2

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of VEGF
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of VEGF

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of BMP-2
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of BMP-2

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of PDGF-BB
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of PDGF-BB

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of osteopontin
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of osteopontin

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of osteocalcin
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of osteocalcin

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)
Plasma concentration of bALP
時間枠:Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

Measure the plasma concentration of bALP

Prior to dosing of ALT-100 on day 1 of each cycle (each cycle is 28 days)

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

捜査官

  • 主任研究者:Daniel Araujo, MD、University of Florida

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)

2027年1月1日

一次修了 (推定)

2028年8月1日

研究の完了 (推定)

2028年8月1日

試験登録日

最初に提出

2026年10月28日

QC基準を満たした最初の提出物

2026年11月3日

最初の投稿 (実際)

2026年11月4日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月4日

QC基準を満たした最後の更新が送信されました

2026年11月3日

最終確認日

2026年10月1日

詳しくは

本研究に関する用語

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

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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