이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

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

2026년 11월 3일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

정황

개입 / 치료

연구 유형

중재적

등록 (추정된)

42

단계

  • 2 단계
  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

남성

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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).

실험적: 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).

실험적: 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).

활성 비교기: 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).

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Incidence of dose limiting toxicities
기간: 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%
기간: 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%
기간: 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
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Maximum plasma concentration of ALT-100
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Daniel Araujo, MD, University of Florida

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2027년 1월 1일

기본 완료 (추정된)

2028년 8월 1일

연구 완료 (추정된)

2028년 8월 1일

연구 등록 날짜

최초 제출

2026년 10월 28일

QC 기준을 충족하는 최초 제출

2026년 11월 3일

처음 게시됨 (실제)

2026년 11월 4일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 4일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 3일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • UF-GU-015

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .