- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00516191
A Phase I/II Study of Liposomal Doxorubicin (Doxil)/Melphalan/Bortezomib (Velcade) in Relapsed/Refractory Multiple Myeloma (DMV)
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
California
-
San Francisco, California, Forenede Stater, 94143
- University of California San Francisco
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Previously diagnosed with multiple myeloma; Durie-Salmon Stage I, II, or III based on standard criteria
- Progressive disease, defined as 25% increase in serum M-protein or Bence Jones protein (an absolute increase of 0.5 gram/dL serum M-protein or at least 200 mg/24 hours of urine light chain excretion). For non-secretory multiple myeloma, progressive disease is defined as bone marrow biopsy with >25% increase in plasma cells or an absolute increase of at least 10% over prior known level. Alternatively, development of new or worsening of existing lytic bone lesions or soft tissue plasmacytomas, or hypercalcemia or relapse from CR.
- 18 year or older and willing and able to comply with the protocol requirements.
- Patient has signed informed consent.
- Unless a female patient is post-menopausal or surgically sterilized, must be willing to use an acceptable method of birth control (hormonal contraceptive, intrauterine device, diaphragm, with spermicide, condom with spermicide, or abstinence) for the duration of the study.
- Male patient must agree to use an acceptable method for contraception for the duration of the study.
- ECOG performance Status of < or equal to 2.
- Life expectancy is at least 3 months.
Initial Required Laboratory Values within 14 days of baseline i.e. Cycle 1, Day 1 (note that renal insufficiency, including dialysis dependence is permissable):
- ANC>1,000uL without the use of colony stimulating factors
- Platelets >50,000/L without transfusion support 7 days before the test
- Bilirubin < or equal to 2.0 mg/dL
- AST < or equal to 4 x upper limit of normal
Prior therapy: Patient must have had at least 2 prior therapeutic regimens as defined below for treatment of multiple myeloma
- Biologic therapy:
Prior nonmyeloablative transplantation allowed provided patient does not have significant graft-versus-host disease and is off aggressive immunosuppressive therapy for at least 30 days. Low dose immunosuppression is allowed (i.e. Prednisone at dose < or equal to 10 mg daily, low dose tacrolimus (subtherapeutic levels) or other agents with equivalent low-dose immunosuppression).
- Chemotherapy:
- Mobilization with chemotherapy followed by either single or tandem autologous transplantation is counted as 1 prior regimen.
- Mobilization with chemotherapy followed by autologous and subsequent nonmyeloablative allogenic transplantation is counted as 1 prior regimen.
- Any combination of drugs given concurrently is counted as a single regimen.
Exclusion Criteria:
- Pregnant or breast-feeding
- History of allergic reaction to compounds containing boron or mannitol.
- Active uncontrolled viral (including HIV), bacterial, or fungal infection.
- Grade III or IV toxicity due to previous anti-neoplastic therapy (except alopecia).
- Grade > or equal to 2 motor or sensory neuropathy as defined by the NCI Common Toxicity Criteria (NCI CTC):
- Grade 2: Either mild objective weakness or objective sensory loss/parasthesia (including tingling) that interferes with function, but not interfering with ADLs.
- Grade 3: Objective weakness or sensory loss/parasthesia interfering with ADLs.
- Grade 4: Paralysis or permanent sensory loss that interferes with function.
- Myocardial infarction within 6 months of enrollment or New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, severe uncontrolled arrhythmias, or electrocardiographic evidence of acute ischemia.
- For any patients whose lifetime cumulative doxorubicin dose exceeds 400 mg/m(2), patients with LVEF < or equal to 35% by MUGA are excluded. In other patients, MUGA is not required but if performed, LVEF must be > or equal to 35%.
- Concurrent administration of liposomal doxorubicin, melphalan, and bortezomib (single or two drug combinations of these are permissable).
- Less than 3 weeks since most recent chemotherapy or concurrent chemotherapy.
- Use of corticosteroids (>10 mg prednisone/day or equivalent).
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
--To evaluate the safety and tolerability of four dose levels of liposomal doxorubicin, melphalan, and bortezomib in patients with relapsed/refractory MM and to identify a maximum tolerated dose of this combination.
Tidsramme: 6 years
|
6 years
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
--To determine the efficacy of DMV therapy --Tabulate all the toxicities of DMV at the MTD by NCI criteria
Tidsramme: 6 years
|
6 years
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Thomas G. Martin, M.D., University of California, San Francisco
Publikationer og nyttige links
Hjælpsomme 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 (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Hjerte-kar-sygdomme
- Karsygdomme
- Sygdomme i immunsystemet
- Neoplasmer efter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Immunproliferative lidelser
- Hæmatologiske sygdomme
- Hæmoragiske lidelser
- Hæmostatiske lidelser
- Paraproteinæmier
- Blodproteinforstyrrelser
- Myelomatose
- Neoplasmer, Plasmacelle
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Enzymhæmmere
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Antineoplastiske midler, Alkylering
- Alkyleringsmidler
- Myeloablative agonister
- Topoisomerase II-hæmmere
- Topoisomerasehæmmere
- Antibiotika, antineoplastisk
- Melphalan
- Bortezomib
- Doxorubicin
- Liposomal doxorubicin
Andre undersøgelses-id-numre
- UC-2408
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 Myelomatose
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Guangzhou Bio-gene Technology Co., LtdTrukket tilbageMultiple myeloma -ildfast
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Zhongshan Hospital (Xiamen), Fudan UniversityIkke rekrutterer endnuMyelomprogression | Multiple myeloma -ildfast
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University Health Network, TorontoIkke rekrutterer endnuMyelom i tilbagefald | Multiple myeloma -ildfastCanada
-
Baskent UniversityIkke rekrutterer endnuMULTIPL SKLEROSETyrkiet (Türkiye)
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Minsk Scientific-Practical Center for Surgery,...RekrutteringAnti-BCMA CAR-T-celleterapi for voksne med tilbagevendende eller refraktær myelomatose (MSTH-CAR001)Multiple myeloma -ildfastHviderusland
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HuniLife Biotechnology, Inc.Tilmelding efter invitationMultiple myeloma -ildfastTaiwan
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Hebei Senlang Biotechnology Inc., Ltd.Peking University People's Hospital; Institute of Hematology & Blood Diseases...Ikke rekrutterer endnuMyelom i tilbagefald | Multiple myeloma -ildfast
-
PETHEMA FoundationRekrutteringDe novo multiple myeloma | Anitocabtagene AutoleucelSpanien
-
CellCentric Ltd.RekrutteringMyelom i tilbagefald | Multiple myeloma -ildfastForenede Stater, Det Forenede Kongerige
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CHU de Quebec-Universite LavalRekrutteringRecidiverende myelomatose | Multiple myeloma -ildfastCanada
Kliniske forsøg med Liposomal Doxorubicin/Melphalan/Bortezomib
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University of California, San FranciscoAfsluttetMyelomatose | PatientdeltagelseForenede Stater
-
Herbert Irving Comprehensive Cancer CenterNational Cancer Institute (NCI)UkendtMyelom og plasmacelle-neoplasmaForenede Stater
-
University of Wisconsin, MadisonNational Cancer Institute (NCI)AfsluttetUspecificeret fast tumor hos voksne, protokolspecifikForenede Stater
-
Johnson & Johnson Pharmaceutical Research & Development...Centocor Ortho Biotech Services, L.L.C.Trukket tilbage
-
Janssen Research & Development, LLCAfsluttetMyelomatoseAustralien, Frankrig, Polen, Det Forenede Kongerige, Forenede Stater, Spanien, Israel, Portugal, Sydafrika, Canada, Holland, Belgien, Singapore, Den Russiske Føderation, Tjekkiet, Argentina, Østrig
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Millennium Pharmaceuticals, Inc.Trukket tilbageLivmoderhalskræftItalien, Schweiz
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National Cancer Institute (NCI)AfsluttetAvanceret primær leverkræft hos voksne | Lokaliseret ikke-operabel primær leverkræft hos voksne | Tilbagevendende primær leverkræft hos voksne | Voksen primært hepatocellulært karcinomForenede Stater
-
National Cancer Institute (NCI)AfsluttetDS Stadie I Plasmacellemyelom | DS Stage II Plasmacellemyelom | DS trin III PlasmacellemyelomForenede Stater
-
National Cancer Institute (NCI)Southwest Oncology GroupAfsluttetTilbagevendende spytkirtelkræft | Tilbagevendende adenoid cystisk karcinom i mundhulen | Stadie III adenoid cystisk karcinom i mundhulen | Stadie III spytkirtelkræft | Stadie IV adenoid cystisk karcinom i mundhulen | Stadie IV spytkirtelkræft | Spytkirtel Adenoid Cystisk CarcinomForenede Stater
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Seoul National University HospitalUkendtSerøst karcinom af høj grad | Ovarie neoplasma epitelialKorea, Republikken