A Phase 1 Study of Nivolumab (BMS-936558) in Subjects With Advanced or Recurrent Malignancies (MDX1106-03)
1 grudnia 2021 zaktualizowane przez: Bristol-Myers Squibb
A Phase 1, Open-Label, Multicenter, Multidose, Dose Escalation Study of BMS-936558 (Nivolumab) in Subjects With Selected Advanced or Recurrent Malignancies
The purpose of this study is to determine the safety and effectiveness of MDX-1106 in patients with certain types of cancer.
Another purpose is to determine how MDX-1106 is absorbed and distributed within the body, and how it's eventually eliminated.
Przegląd badań
Status
Zakończony
Warunki
Typ studiów
Interwencyjne
Zapisy (Rzeczywisty)
395
Faza
- Faza 1
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
-
-
Arizona
-
Scottsdale, Arizona, Stany Zjednoczone, 85258
- Pinnacle Oncology Hematology
-
-
Connecticut
-
New Haven, Connecticut, Stany Zjednoczone, 06520
- Yale University School Of Medicine
-
-
Florida
-
Tampa, Florida, Stany Zjednoczone, 33612-9497
- H. Lee Moffitt Cancer Center & Research Institute
-
-
Maryland
-
Baltimore, Maryland, Stany Zjednoczone, 21231
- Johns Hopkins University
-
-
Massachusetts
-
Boston, Massachusetts, Stany Zjednoczone, 02215
- Beth Israel Deaconess Medical Center
-
Boston, Massachusetts, Stany Zjednoczone, 02215
- Dana Farber Cancer Institute
-
Boston, Massachusetts, Stany Zjednoczone, 02215
- Massachusetts General Hospital
-
-
Michigan
-
Ann Arbor, Michigan, Stany Zjednoczone, 48109
- University of Michigan Cancer Center
-
-
New York
-
New York, New York, Stany Zjednoczone, 10065
- Memorial Sloan Kettering Nassau
-
-
North Carolina
-
Huntersville, North Carolina, Stany Zjednoczone, 28078
- Carolina Biooncology Institute
-
-
Ohio
-
Cincinnati, Ohio, Stany Zjednoczone, 45219
- Christ Hospital
-
-
Tennessee
-
Nashville, Tennessee, Stany Zjednoczone, 37203
- Sarah Cannon Research Institute
-
Nashville, Tennessee, Stany Zjednoczone, 37232
- Vanderbilt-Ingram Cancer Ctr
-
-
Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
18 lat i starsze (Dorosły, Starszy dorosły)
Akceptuje zdrowych ochotników
Nie
Płeć kwalifikująca się do nauki
Wszystko
Opis
For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com
Inclusion Criteria:
- Subjects must have mCRPC,RCC, MEL, Non-small-cell lung cancer (NSCLC), or Colorectal Cancer (CRC), that is advanced (non-resectable), or recurrent and for which no alternative, curative standard exists
- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2
- Must have at least 1 measurable lesion
- Subjects with mCRPC and with only non-measurable bone lesions must have either progression new lesions or have Prostate-specific antigen (PSA) progression within the 6-week period before study administration
- At least 1 and up to 5 prior systemic therapies for advanced/recurrent disease
- Prior treated brain or meningeal metastases must be without Magnetic resonance imaging (MRI) evidence of progression for at least 8 weeks and off immunosuppressive doses of systemic steroids for at least 2 weeks before study drug administration
- Prior systemic radiation therapy must have been completed at least 4 weeks before study drug administration. Prior focal radiotherapy completed at least 2 weeks prior to study drug administration
- Immunosuppressive doses of systemic medications, such as steroids or absorbed topical steroids must be discontinued at least 2 weeks before study drug administration
- Prior surgery that required general anesthesia must be completed at least 2 weeks before study drug administration. Surgery requiring local/epidural anesthesia must be completed at least 72 hours before study drug administration
Exclusion Criteria:
- History of severe hypersensitivity reactions to other Monoclonal antibody (mAb)s
- Subjects with any active autoimmune disease or a documented history of autoimmune disease, or history of syndrome that required systemic steroids or immunosuppressive medications, except for subjects with vitiligo or resolved childhood asthma/atopy
- Prior therapy with an anti-Programmed death-1 (PD-1), anti-PD-L1, anti-PD-L2, or anti- Cytotoxic t-lymphocyte antigen-4 (CTLA-4) antibody (or any other antibody targeting T cell co-stimulation pathways)
- Known history of Human Immunodeficiency Virus
- Active infection requiring therapy, positive tests for Hepatitis B surface antigen or Hepatitis C ribonucleic acid (RNA)
- Underlying medical conditions that will make the administration of study drug hazardous
- Concurrent medical condition requiring the use of immunosuppressive medications, or immunosuppressive doses of systemic or absorbable topical corticosteroids
- Use of other investigational drugs (drugs not marketed for any indication) within 28 days or at least 5 half-lives (whichever is longer) before study drug administration
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nielosowe
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Melanoma - BMS-936558 (MDX-1106)
|
Solution, Intravenous, 0.1 mg/kg - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 1 - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
|
|
Eksperymentalny: RCC - BMS-936558 (MDX-1106)
|
Solution, Intravenous, 0.1 mg/kg - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 1 - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
|
|
Eksperymentalny: mCRPC - BMS-936558 (MDX-1106)
|
Solution, Intravenous, 0.1 mg/kg - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 1 - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
|
|
Eksperymentalny: NSCLC - BMS-936558 (MDX-1106)
|
Solution, Intravenous, 0.1 mg/kg - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 1 - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
|
|
Eksperymentalny: CRC - BMS-936558 (MDX-1106)
|
Solution, Intravenous, 0.1 mg/kg - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 1 - 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
Solution, Intravenous, 10 mg/kg, Every 2 weeks, 3 years depending on response
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Number of Participants With Severe Adverse Events (AEs), Serious Adverse Events (SAEs), Treatment-Related AEs, Deaths, Discontinuation of Study Drug Due to AEs
Ramy czasowe: Day 1 to 70 days following last dose of study drug up to June 2013, approximately 4 years
|
AE=any new unfavorable symptom, sign or disease or worsening of a preexisting condition that may not have a causal relationship with treatment. SAE=a medical event that at any dose results in death, persistent or significant disability/incapacity or drug dependency/abuse; is life-threatening, an important medical event or a congenital anomaly/birth defect; or requires or prolongs hospitalization. Treatment-related=having certain, probable, possible or missing relationship to study drug. Death=during the study and up to 28 days past study discontinuation. The select AEs were determined using the Medical Dictionary for Regulatory Activities (MedDRA, v15.1) and graded using the Cancer Therapy Evaluation Program Common Terminology Criteria for Adverse Events (CTCAE), Version 3.0. |
Day 1 to 70 days following last dose of study drug up to June 2013, approximately 4 years
|
|
Number of Participants With Abnormal Serum Chemistry Laboratory Values
Ramy czasowe: Day 1 up to June 2013, approximately 4 years
|
Alkaline phosphatase (ALP), Alanine Aminotransferase (ALT), Aspartate Aminotransferase (AST), Creatinine and Total Bilirubin.
National Cancer Institute Common Terminology Criteria (CTC) version (v) 3.0 was used to determine Grade (Gr).
Abnormal values for ALP, ALT and AST were based on grades; Gr 1: > 1.0 - 2.5 * upper limits of normal (ULN); Gr 2: > 2.5 - 5.0 * ULN; Gr 3: > 5.0 - 20.0 * ULN; Gr 4: > 20.0 * ULN.
Abnormal values for Creatinine were based on Gr 1: > 1.0 - 1.5*ULN; Gr 2: > 1.5 - 3.0*ULN; Gr 3: > 3.0 - 6.0*ULN; Gr 4: > 6.0*ULN.
Abnormal values for Total Bilirubin were based on Gr 1: > 1.0 - 1.5 * upper limits of normal (ULN); Gr 2: > 1.5 - 3.0 * ULN; Gr 3: > 3.0 - 10.0 * ULN; Gr 4: > 10.0 * ULN.
|
Day 1 up to June 2013, approximately 4 years
|
|
Number of Participants With Abnormal Hematology Laboratory Values
Ramy czasowe: Day 1 up to June 2013, approximately 4 years
|
Hemoglobin, Lymphocytes, Neutrophils, Platelets and Leukocytes.
National Cancer Institute Common Terminology Criteria (CTC) version (v) 3.0 was used to determine Grade (Gr).
Abnormal values for Hemoglobin were based on Gr 1: 10.0 - less than (<) lower limit of normal (LLN); Gr 2: 8.0 - < 10.0; Gr 3: 6.5 - < 8.0; Gr 4: < 6.5.
Abnormal values for Lymphocytes were based on Gr 1: 0.8 - < 1.5; Gr 2: 0.5 - < 0.8; Gr 3): 0.2 - < 0.5; Gr 4: < 0.2.
Abnormal values for Neutrophils were based on Gr 1: 1.5 - < 2.0; Gr 2: 1.0 - < 1.5; Gr 3: 0.5 - < 1.0; Gr 4: < 0.5.
Abnormal values for Platelets were based on Gr 1: 75.0 - < lower limits of normal (LLN); Gr 2: 50.0 - < 75.0;
Gr 3: 25.0 - < 50.0;
Gr 4: < 25.0.
Abnormal values for Leukocytes were based on Gr 1: 3.0 - < LLN; Gr 2: 2.0 - < 3.0; Gr 3: 1.0 - < 2.0; Gr4: < 1.0.
|
Day 1 up to June 2013, approximately 4 years
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Immunogenicity Assessment
Ramy czasowe: Day 1 up to June 2013, approximately 4 years
|
Classification of participants host immune response was based on the following definitions: Anti-Drug Antibody (ADA) Positive Subjects have with at least one ADA positive sample at any time after initiation of treatment.
ADA positive subjects were further classified into categories with Persistent Positive defined as an ADA positive sample at 2 or more sequential timepoints at least 8 weeks apart.
|
Day 1 up to June 2013, approximately 4 years
|
|
Objective Response Rate
Ramy czasowe: Day 1 up to June 2013, approximately 4 years
|
Tumor response was evaluated by the sponsor based on tumor assessments by the investigator according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.0.
Objective response rate (ORR) was defined as the proportion of participants who's confirmed best overall response (BOR) is either complete (CR) or partial (PR), where the denominator is the number of treated participants in the population of interest.
Response was based on tumor measurements.
Responders= complete response (CR) or partial response (PR).
CR=disappearance of all target and non-target lesions; PR=at least a 30% decrease in the sum of the longest diameter of target lesions, taking as reference the screening sum longest diameter.
95% Confidence intervals (CIs) were computed using the Clopper Pearson method.
|
Day 1 up to June 2013, approximately 4 years
|
|
Duration of Tumor Response
Ramy czasowe: Day 1 up to June 2013, approximately 4 years
|
Duration of tumor response (DOR) was calculated from the first date of response of complete response (CR) or partial response (PR) to the date of the first progressive disease (PD) or the date of death.
Duration of response was censored at the last tumor assessment date if a responder did not have PD or death.
Nonresponders were not included in the analysis.
Median DOR was estimated by Kaplan-Meier analysis.
|
Day 1 up to June 2013, approximately 4 years
|
|
Geometric Mean Maximum Serum Concentration (Cmax)
Ramy czasowe: 1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycles 1 and 3
|
Nivolumab in human serum was assayed by PPD® (Richmond, Virginia) using a cross-validated enzyme-linked immunosorbent assay (ELISA).
Blood samples were assessed at all doses from a subset of participants.
The pharmacokinetic (PK) parameter of Cmax was measured in micrograms per milliliter (µg/mL).
|
1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycles 1 and 3
|
|
Median Time of Maximum Serum Concentration (Tmax)
Ramy czasowe: 1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycles 1 and 3
|
Nivolumab in human serum was assayed by PPD® (Richmond, Virginia) using a cross-validated ELISA.
Blood samples were assessed Blood samples were assessed at all doses from a subset of participants.
The PK parameter of Tmax was measured in hours (h).
|
1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycles 1 and 3
|
|
Geometric Mean Area Under the Curve (AUC[TAU]) in One Dosing Interval Observed Post-Single Dose
Ramy czasowe: 1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycles 1 and 3
|
Nivolumab in human serum was assayed by PPD® (Richmond, Virginia) using a cross-validated ELISA.
Blood samples were assessed at all doses from a subset of participants.
The PK parameter of AUC was measured in micrograms*hours per milliliter (μg*h/mL).
|
1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycles 1 and 3
|
|
Geometric Mean Total Body Clearance of Drug From Serum (CLT)
Ramy czasowe: 1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycle 3
|
Nivolumab in human serum was assayed by PPD® (Richmond, Virginia) using a cross-validated ELISA.
Blood samples Blood samples were assessed at all doses from a subset of participants.
The PK parameter of CLT was measured in milliliters per hour (mL/h).
|
1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycle 3
|
|
Mean Effective Half-life (T-HALFeff)
Ramy czasowe: 1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycle 3
|
Nivolumab in human serum was assayed by PPD® (Richmond, Virginia) using a cross-validated ELISA.
Blood samples were assessed at all doses from a subset of participants.
The PK parameter of T-HALFeff was measured in hours (h).
|
1,4,8,24,48 and 96 hours post-dose timepoints on Day 1 of cycle 3
|
Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Współpracownicy
Publikacje i pomocne linki
Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.
Publikacje ogólne
- Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, McDermott DF, Powderly JD, Sosman JA, Atkins MB, Leming PD, Spigel DR, Antonia SJ, Drilon A, Wolchok JD, Carvajal RD, McHenry MB, Hosein F, Harbison CT, Grosso JF, Sznol M. Five-Year Survival and Correlates Among Patients With Advanced Melanoma, Renal Cell Carcinoma, or Non-Small Cell Lung Cancer Treated With Nivolumab. JAMA Oncol. 2019 Oct 1;5(10):1411-1420. doi: 10.1001/jamaoncol.2019.2187.
- Topalian SL, Sznol M, McDermott DF, Kluger HM, Carvajal RD, Sharfman WH, Brahmer JR, Lawrence DP, Atkins MB, Powderly JD, Leming PD, Lipson EJ, Puzanov I, Smith DC, Taube JM, Wigginton JM, Kollia GD, Gupta A, Pardoll DM, Sosman JA, Hodi FS. Survival, durable tumor remission, and long-term safety in patients with advanced melanoma receiving nivolumab. J Clin Oncol. 2014 Apr 1;32(10):1020-30. doi: 10.1200/JCO.2013.53.0105. Epub 2014 Mar 3.
- Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, McDermott DF, Powderly JD, Carvajal RD, Sosman JA, Atkins MB, Leming PD, Spigel DR, Antonia SJ, Horn L, Drake CG, Pardoll DM, Chen L, Sharfman WH, Anders RA, Taube JM, McMiller TL, Xu H, Korman AJ, Jure-Kunkel M, Agrawal S, McDonald D, Kollia GD, Gupta A, Wigginton JM, Sznol M. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med. 2012 Jun 28;366(26):2443-54. doi: 10.1056/NEJMoa1200690. Epub 2012 Jun 2.
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
30 października 2008
Zakończenie podstawowe (Rzeczywisty)
4 lutego 2013
Ukończenie studiów (Rzeczywisty)
22 grudnia 2020
Daty rejestracji na studia
Pierwszy przesłany
4 sierpnia 2008
Pierwszy przesłany, który spełnia kryteria kontroli jakości
7 sierpnia 2008
Pierwszy wysłany (Oszacować)
8 sierpnia 2008
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
3 grudnia 2021
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
1 grudnia 2021
Ostatnia weryfikacja
1 listopada 2021
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Nowotwory według typu histologicznego
- Nowotwory
- Nowotwory urologiczne
- Nowotwory układu moczowo-płciowego
- Nowotwory według lokalizacji
- Choroby nerek
- Choroby Urologiczne
- Rak gruczołowy
- Rak
- Nowotwory gruczołowe i nabłonkowe
- Nowotwory nerek
- Rak, Komórka Nerki
- Molekularne mechanizmy działania farmakologicznego
- Środki przeciwnowotworowe
- Środki przeciwnowotworowe, immunologiczne
- Inhibitory immunologicznego punktu kontrolnego
- Niwolumab
Inne numery identyfikacyjne badania
- CA209-003
- MDX1106-03 (Inny identyfikator: BMS)
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Tak
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
produkt wyprodukowany i wyeksportowany z USA
Nie
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .