- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01778439
A Dose Escalation Study of OMP-52M51 in Subjects With Solid Tumors
A Phase 1 Dose Escalation Study of OMP-52M51 in Subjects With Solid Tumors
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
California
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San Francisco, California, Forenede Stater, 94115
- University of California, San Francisco/Helen Diller Cancer Institute
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Colorado
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Aurora, Colorado, Forenede Stater, 80045
- University of Colorado Denver -RCI-South Tower
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Michigan
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Detroit, Michigan, Forenede Stater, 48201
- Karmanos Cancer Institute (KCI)
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Detroit, Michigan, Forenede Stater, 48201
- Wayne State University/Oncology Karmanos Cancer Institute
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Texas
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Houston, Texas, Forenede Stater, 77030
- The University of Texas MD Anderson Cancer Center
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San Antonio, Texas, Forenede Stater, 78229
- South Texas Accelerated Research Therapeutics, LLC
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-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
Subjects must meet all of the following criteria to be eligible for the study:
- Age >18 years
- ECOG performance status <2 (see Appendix B)
- Solid tumor malignancy for which there is no remaining standard therapy or either refuse or are not considered to be candidates for any remaining standard therapy.
- Must have a tumor that is measurable or evaluable per RECIST v1.1 in the dose escalation phase. In the expansion cohort(s), subjects must have measurable disease.
- Subjects must have Formalin-Fixed, Paraffin-Embedded (FFPE) tissue available either archived or fresh core or punch needle biopsied at study entry (two fresh cores/punches preferred whenever possible) for determination of Notch1 pathway activation status.
- Must have received their last chemotherapy, biologic, radiotherapy, or investigational therapy at least 4 weeks prior to enrollment; 6 weeks if the last regimen included BCNU or mitomycin C.
Subjects must have normal organ and marrow function as defined below:
- Absolute neutrophil count >1500/mL without growth factor support in the past 7 days
- Platelets >100,000/mL without transfusions in the past 7 days
- Total bilirubin <1.5 X institutional upper limit of normal (ULN) (<2X ULN for subjects with Gilbert's syndrome)
- AST (SGOT) and ALT (SGPT) <3 X institutional ULN (for subjects with hepatic involvement <5 X institutional ULN but cannot be associated with elevated bilirubin)
- PT/INR and aPTT within 1.5 X institutional ULN
- Creatinine <1.5 X institutional ULN OR
- Creatinine clearance >60 mL/min/1.73 m2 for subjects with creatinine levels above institutional normal
- Normal Ejection Fraction (>50%) on ECHO scan or MUGA
- Women of childbearing potential must have had a prior hysterectomy or have a negative serum pregnancy test and be using adequate contraception prior to study entry and must agree to use adequate contraception from study entry through at least 6 months after discontinuation of study drug. Men must also agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and from study entry through at least 6 months after discontinuation of study drug. Should a woman enrolled in the study or a female partner of a man enrolled in the study become pregnant or suspect she is pregnant while participating in this study or within 6 months after discontinuation of study, she should inform the Investigator immediately.
- Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
Subjects who meet any of the following criteria will not be eligible for participation in the study:
- Currently receiving any therapeutic treatment for their malignancy including other investigational agents
- Prior treatment with gamma secretase inhibitors or other Notch 1 inhibitors
- Uncontrolled seizure disorder, active neurologic disease, or active CNS involvement except for individuals who have previously-treated CNS metastases, are asymptomatic, and have no requirement for higher doses of corticosteroids (> prednisone 10mg orally per day) or anti-seizure medication for at least 4 weeks prior to first dose of study drug.
- History of a Grade 4 allergic reaction attributed to humanized or human monoclonal antibody therapy
- Significant intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- Pregnant women or nursing women
- Ongoing malignancies or malignancies in remission <3 years other than the malignancies included in this trial. Patients with history of known squamous cell skin cancers within the past 3 years will not be included in this trial. The following prior malignancies are allowable irrespective of when they occurred: in situ carcinoma of the cervix, in situ ductal breast cancer, and low-grade local bladder cancer.
- Subjects with known HIV infection
- Known bleeding disorder or coagulopathy
- Known endobronchial lesions and/or lesions infiltrating major pulmonary vessels.
- Hemoptysis in excess of 2.5 mL(or one-half teaspoon) within 8 weeks of first dose of study drug.
- Subjects receiving heparin, warfarin, or other similar anticoagulants, except for subjects on low molecular weight heparin for DVT/PE prophylaxis. Note: Subjects may be receiving low-dose aspirin and/or non-steroidal anti-inflammatory agents.
- New York Heart Association Classification II, III, or IV (see Appendix D)
Subjects with poorly controlled blood pressure (defined as systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg) that is not responsive to medical therapy. Subjects taking antihypertensive medications must be taking ≤2 medications to obtain this level of blood pressure control.
NOTE: Initiation or adjustment of antihypertensive medication(s) is permitted prior to study entry.
- Subjects with ECG evidence of ischemia or ≥Grade 2 ventricular arrhythmia, subjects who have a history of acute myocardial infarction within 6 months, or subjects with unstable angina.
Subjects with known clinically significant gastrointestinal disease including, but not limited to:
- inflammatory bowel disease
- active peptic ulcer disease
- known intraluminal metastatic lesion(s) with risk of bleeding
- history of abdominal fistula, GI perforation, or intra-abdominal abscess within 28 days prior to beginning study treatment
- Subjects with diarrhea at time of enrollment or have an ongoing requirement for anti diarrheal therapy
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: OMP-52M51
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Safety profile of OMP-52M51 in subjects with relapsed or refractory solid tumors
Tidsramme: Subjects will be assessed for DLTs from Days 0-29. Adverse events will be reported through 30 days after the last dose
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Subjects will be assessed for DLTs from Days 0-29. Adverse events will be reported through 30 days after the last dose
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Pharmacokinetics (PK) of OMP-52M51 in subjects with relapsed or refractory solid tumors
Tidsramme: PK analyses at various time points following the 1st and 2nd doses, immediately pre and post-dose for all subsequent doses at treatment term, every 4 weeks after discontinuation of study drug or 12 weeks
|
Apparent half life, AUC, clearance, volume of distribution
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PK analyses at various time points following the 1st and 2nd doses, immediately pre and post-dose for all subsequent doses at treatment term, every 4 weeks after discontinuation of study drug or 12 weeks
|
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Immunogenicity
Tidsramme: Assessed at baseline, prior to each dose, at treatment termination and every 4 weeks after the discontinuation of the study drug for 12 weeks.
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Assessed at baseline, prior to each dose, at treatment termination and every 4 weeks after the discontinuation of the study drug for 12 weeks.
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|
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Preliminary Efficacy
Tidsramme: Evaluation for response will be assessed on day 70 of study and every 8 weeks (or 9 weeks for Q3W schedule) thereafter and will be based on RECIST v1.1.
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Evaluation for response will be assessed on day 70 of study and every 8 weeks (or 9 weeks for Q3W schedule) thereafter and will be based on RECIST v1.1.
|
Samarbejdspartnere og efterforskere
Sponsor
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 52M51-002
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
produkt fremstillet i og eksporteret fra U.S.A.
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Kliniske forsøg med Recidiverende eller refraktære solide tumorer
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Nantes University HospitalTrukket tilbageCD22+ Relapsed/Refractory B-ALLFrankrig
-
Changhai HospitalRui Therapeutics Co., LtdRekrutteringRelapseret/Refraktær Immun Nefropati | Relapsed/Refractory Immune-mediated Kidney DiseaseKina
-
Shanghai Pudong HospitalUTC Therapeutics Inc.Trukket tilbageMesothelin-positive Advanced Refractory Solid TumorsKina
-
Memorial Sloan Kettering Cancer CenterRekrutteringSolid tumor | Solid tumor, voksen | Solid tumor, uspecificeret, voksenForenede Stater
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Memorial Sloan Kettering Cancer CenterLincoln Medical and Mental Health CenterRekrutteringSolid tumor | Solid tumor, voksen | Solid tumor, uspecificeret, voksenForenede Stater, Puerto Rico
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Memorial Sloan Kettering Cancer CenterLincoln Medical and Mental Health CenterRekrutteringSolid tumor | Solid tumor, voksen | Solid tumor, uspecificeret, voksenForenede Stater, Puerto Rico
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Memorial Sloan Kettering Cancer CenterRekrutteringSolid tumor | Solid tumor, voksenForenede Stater
-
Avelos Therapeutics Inc.RekrutteringSolid tumor | Solid tumorkræft | Solid tumor, voksen | Solid tumor, uspecificeret, voksen | Tumor, fast | Solid tumor i avanceret scene | Faste tumorer, der er ildfast til standardterapiKorea, Republikken
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Sorrento Therapeutics, Inc.Trukket tilbageSolid tumor | Recidiverende solid tumor | Refraktær tumor
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Neurogene Inc.Merck Sharp & Dohme LLCAfsluttetSolid tumor | Avanceret solid tumorForenede Stater, Australien, Canada
Kliniske forsøg med OMP-52M51
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OncoMed Pharmaceuticals, Inc.AfsluttetTilbagefaldende eller refraktære lymfoide maligniteterForenede Stater
-
M.D. Anderson Cancer CenterAfsluttetAdenoid cystisk karcinomForenede Stater
-
OncoMed Pharmaceuticals, Inc.AfsluttetMetastatisk tyktarmskræftForenede Stater
-
Can Tho University of Medicine and PharmacyRekrutteringMedicinsk Uddannelse | Klinisk Undervisning | SengekantundervisningVietnam
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OncoMed Pharmaceuticals, Inc.AfsluttetFaste tumorerForenede Stater
-
OncoMed Pharmaceuticals, Inc.Novotech (Australia) Pty LimitedAfsluttetKolorektal cancerAustralien, New Zealand
-
OncoMed Pharmaceuticals, Inc.BayerAfsluttetFaste tumorerForenede Stater
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OncoMed Pharmaceuticals, Inc.AfsluttetMetastatisk kræft | Lokalt avanceret malignt neoplasmaForenede Stater
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OncoMed Pharmaceuticals, Inc.AfsluttetFaste tumorerForenede Stater
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OncoMed Pharmaceuticals, Inc.AfsluttetRefraktære faste tumorer | Avancerede recidiverende tumorerForenede Stater