ALT-100 Monoclonal Antibody (mAb) in Bone-Predominant Metastatic Androgen Pathway Modulation Resistant (APMR) Prostate Cancer -- The ALTAR-100 Trial
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.
Przegląd badań
Status
Status
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Typ studiów
Typ studiów
Zapisy (Szacowany)
Zapisy
Faza
Faza
- Faza 2
- Faza 1
Kontakty i lokalizacje
Kontakt w sprawie studiów
Kontakt w sprawie studiów
- Nazwa: Alexandra Leggett
- Numer telefonu: 352-273-9785
- E-mail: agmueller@ufl.edu
Kryteria uczestnictwa
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
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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:
- 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,
- 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,
- For PSMA-PET: Two new PSMA-avid lesions, or
- 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
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Life expectancy ≥6 months
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Adequate organ and marrow function defined as:
- ANC ≥1,500/µL
- Platelets ≥100,00/µL
- Hemoglobin ≥9.0 g/dL without transfusion within 14 days
- Total bilirubin ≤1.5 x ULN (≤ 3 x ULN for Gilbert's)
- AST and ALT ≤3 x ULN
- 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.
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Written informed consent obtained from the subject and the subject agrees to comply with all the study-related procedures.
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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.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Zadanie sekwencyjne
- Maskowanie: Brak (otwarta etykieta)
Liczba ramion
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
|---|---|
|
Eksperymentalny: 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). |
|
Eksperymentalny: 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). |
|
Eksperymentalny: 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). |
|
Aktywny komparator: 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). |
Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Incidence of dose limiting toxicities
Ramy czasowe: 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%
Ramy czasowe: 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%
Ramy czasowe: 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
Ramy czasowe: 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
|
Miary wyników drugorzędnych
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Maximum plasma concentration of ALT-100
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
|
Współpracownicy i badacze
Sponsor
Sponsor
Śledczy
Śledczy
- Główny śledczy: Daniel Araujo, MD, University of Florida
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Rozpoczęcie studiów
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
Ukończenie studiów (Szacowany)
Ukończenie studiów
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Choroby układu moczowo-płciowego
- Choroby narządów płciowych
- Nowotwory narządów płciowych, mężczyzna
- Nowotwory układu moczowo-płciowego
- Nowotwory według lokalizacji
- Nowotwory
- Choroby narządów płciowych, mężczyzna
- Choroby prostaty
- Choroby układu moczowo-płciowego u mężczyzn
- Nowotwory prostaty
- AMR Syndrome
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- UF-GU-015
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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