- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT03560752
Kantasoluluovuttajien CMV-MVA Triplex -rokote CMV-viremian ehkäisyyn potilailla, joilla on verisyöpä ja joille tehdään luovuttajan kantasolusiirto
Kantasoluluovuttajien CMV-MVA Triplex -rokote CMV-spesifisen immuniteetin parantamiseksi ja CMV-viremian estämiseksi vastaanottajilla kantasolusiirron jälkeen
This phase II trial studies how well multi-peptide CMV-modified vaccinia Ankara (CMV-MVA Triplex) vaccination of stem cell donors works in preventing cytomegalovirus (CMV) viremia in participants with blood cancer undergoing donor stem cell transplant. Giving a vaccine to the donors may boost the recipient's immunity to this virus and reduce the chance of CMV disease after transplant.
Tutkimuksen yleiskatsaus
Tila
Ehdot
- Hematopoieettinen ja lymfoidisolukasvain
- Hodgkinin lymfooma
- Myelofibroosi
- Krooninen lymfosyyttinen leukemia
- Non-Hodgkin-lymfooma
- Myelodysplastinen oireyhtymä
- Myelodysplastinen/myeloproliferatiivinen kasvain
- Akuutti myelooinen leukemia remissiossa
- Akuutti lymfoblastinen leukemia remissiossa
- Sytomegalovirus positiivinen
- Luovuttaja
- Hematopoieettisten solujen siirron vastaanottaja
- Nopeutettu vaihe CML, BCR-ABL1 positiivinen
- Kroonisen vaiheen CML, BCR-ABL1 positiivinen
Interventio / Hoito
Yksityiskohtainen kuvaus
PRIMARY OBJECTIVES:
I. Establish the feasibility and safety of priming CMV immunity in donors by Triplex vaccination prior to peripheral blood stem cell (PBSC) harvest.
SECONDARY OBJECTIVES:
I. Examine if Triplex vaccination of hematopoietic stem cell transplant (HCT) donors has an impact on CMV events.
OUTLINE:
Donors receive multi-peptide CMV-modified vaccinia Ankara vaccine injection between days -60 and -10 prior to granulocyte colony stimulating factor mobilization. Participants undergo hematopoietic cell transplantation on day 0.
After completion of study treatment, participants are followed up for 1 year.
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Vaihe 1
Yhteystiedot ja paikat
Opiskelupaikat
-
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California
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Duarte, California, Yhdysvallat, 91010
- City of Hope Medical Center
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-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- DONOR: Ability to comprehend the investigational nature of the study and provide informed consent
- DONOR: Willing to receive Triplex vaccination, a minimum of 14 days prior to the PBSC collection
- DONOR VACCINATION: Donors are eligible to be vaccinated prior to the determination of their human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV) and human T-cell lymphotropic virus (HTLV) status. The exclusion criteria for transplant is independent of eligibility for vaccination and is determined by the exclusion criteria for transplant from donors
- RECIPIENT: All subjects must have the ability to understand and the willingness to sign a written informed consent
- RECIPIENT: Participant must be willing to comply with study and/or follow-up procedures, including willingness to be followed for one year post-HCT
- RECIPIENT: Age 18 to 75 years
- RECIPIENT: Planned HCT for the treatment of the following hematologic malignancies: lymphoma (Hodgkin and non-Hodgkin), myelodysplastic syndrome, acute lymphoblastic leukemia in first or second remission, acute myeloid leukemia in first or second remission, chronic myelogenous leukemia (in first chronic or accelerated phase, or in second chronic phase), chronic lymphocytic leukemia, myeloproliferative disorders and myelofibrosis (City of Hope [COH] only). Patients with multiple myeloma are excluded
- RECIPIENT: CMV seropositive
- RECIPIENT: Planned related HCT with 8/8 (A, B, C, DRB1) high resolution HLA donor allele matching
- RECIPIENT: Conditioning and immunosuppressive regimens according to institutional guidelines are permitted
- RECIPIENT: Negative serum or urine beta-human chorionic gonadotropin (HCG) test (female patient of childbearing potential only) within two weeks of registration
- RECIPIENT: Seronegative for HIV, HCV and active HBV (surface antigen negative) within 2 months of registration
- RECIPIENT: Agreement by females of childbearing potential and males with partners of childbearing potential to use effective contraception (hormonal or barrier method or abstinence) prior to study entry and for up to 90 days post-HCT. Should a woman become pregnant or suspect that she is pregnant while participating on the trial, she should inform her treating physician immediately
Exclusion Criteria:
- TRANSPLANT FROM DONOR: Unfit to undergo standard stem cell mobilization and apheresis e.g. abnormal blood counts, history of stroke, uncontrolled hypertension
- TRANSPLANT FROM DONOR: Sickling hemoglobinopathy including HbSS, HbAS, HbSC
- TRANSPLANT FROM DONOR: Positive for human immunodeficiency virus (HIV), active hepatitis B (hepatitis B virus [HBV]), hepatitis C (hepatitis C virus [HCV]) or human T-cell lymphotropic virus (HTLV-I/II). This holds true even if donors have been already vaccinated according to criteria for donor vaccination
- TRANSPLANT FROM DONOR: Donors with impaired cardiac function are excluded. Electrocardiography is routine for potential HCT donors over 60 years old and those with a history of heart disease. Subjects in whom cardiac function is abnormal (excluding 1st degree branch block, sinus brachycardia, sinus tachycardia or non-specific T wave changes) are ineligible for Triplex vaccination
- TRANSPLANT FROM DONOR: Severe psychiatric illness. Mental deficiency sufficiently severe as to make compliance with the donation procedure unlikely, and making informed consent impossible
- RECIPIENT: Any prior investigational CMV vaccine
- RECIPIENT: Experimental anti-CMV chemotherapy in the last 6 months
- RECIPIENT: Planned medications from the time of HCT to day 70 post-HCT
- RECIPIENT: Live attenuated vaccines
- RECIPIENT: Medically indicated subunit (Engerix-B for HBV; Gardasil for human papillomavirus [HPV]) or killed vaccines (e.g. influenza, pneumococcal, or allergy treatment with antigen injections)
- RECIPIENT: Allergy treatment with antigens injections
- RECIPIENT: Alemtuzumab or any equivalent in vivo T-cell depleting agent
- RECIPIENT: Antiviral medications with known therapeutic effects on CMV such as ganciclovir (GCV)/valganciclovir (VAL), FOS, Cidofovir, CMX-001, maribavir. Acyclovir has no known therapeutic efficacy against CMV and is allowable as standard of care to prevent Herpes simplex virus (HSV)
- RECIPIENT: Prophylactic therapy with CMV immunoglobulin or prophylactic antiviral CMV treatment (Letermovir is permitted). EXCEPT for low risk patients [8/8 high resolution HLA donor allele matching HCT])
- RECIPIENT: Other investigational product - concurrent enrollment in other clinical trials using any investigational new drug (IND) drugs with unknown effects on CMV or with unknown toxicity profiles is prohibited
- RECIPIENT: Other medications that might interfere with the evaluation of the investigational product
- RECIPIENT: Diagnosis with autoimmune disease
- RECIPIENT: Pregnant women and women who are lactating. The risks of CMV-MVA-Triplex to pregnant women are unknown. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother. Breastfeeding should be discontinued if the mother is enrolled on this study
- RECIPIENT: Any other condition that would, in the investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns or compliance with clinical study procedures, e.g., social/ psychological issues, etc
- RECIPIENT: Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Tukevaa hoitoa
- Jako: Ei satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: Donor (multi-peptide CMV-modified vaccinia Ankara vaccine)
Donors receive multi-peptide CMV-modified vaccinia Ankara vaccine injection between days -60 and -10 prior to granulocyte colony stimulating factor mobilization. |
Given via injection
Muut nimet:
|
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Kokeellinen: Receipient (multi-peptide CMV-modified vaccinia Ankara vaccine)
Participants undergo hematopoietic cell transplantation on day 0 and receive multi-peptide CMV-modified Vaccinia Ankara vaccine injection on days 28 and 56. |
Given via injection
Muut nimet:
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Delayed Engraftment
Aikaikkuna: Up to 1 year from stem cell infusion.
|
Time to neutrophil engraftment was defined as days from stem cell infusion to the first of three consecutive days of absolute neutrophil count ≥0.5 x 109/L. Delayed engraftment was defined as ≥20 days to neutrophil recovery. |
Up to 1 year from stem cell infusion.
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Severe (Grade III-IV) Acute Graft Versus Host Disease
Aikaikkuna: Up to 6 months from stem cell infusion
|
Acute graft versus host disease (aGvHD) happens within days or as late as 6 months after allogeneic transplants. The three main tissues that acute GVHD affects are the skin, liver, and gastrointestinal tract. |
Up to 6 months from stem cell infusion
|
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Number of Recipients With Grade 3-4 Adverse Events
Aikaikkuna: Up to 1 year from stem cell infusion.
|
Toxicities were assessed in recipients by Common Terminology Criteria for Adverse Events version 4.0. |
Up to 1 year from stem cell infusion.
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Number of Donors With Grade 2-3 Adverse Events
Aikaikkuna: Up to 6 months after G-CSF mobilization
|
Toxicities were assessed in recipients by Common Terminology Criteria for Adverse Events version 4.0. |
Up to 6 months after G-CSF mobilization
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100-Day Non-Relapse Mortality (NRM)
Aikaikkuna: From stem cell infusion up to 100 days post-HSCT (hematopoietic stem cell transplantation).
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NRM was defined as death without recurrent or progressive disease after allogeneic transplant. Probabilities of NRM were estimated with the use of cumulative incidence curves, with relapse viewed as a competing risk. |
From stem cell infusion up to 100 days post-HSCT (hematopoietic stem cell transplantation).
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Yhteistyökumppanit ja tutkijat
Sponsori
Yhteistyökumppanit
Tutkijat
- Päätutkija: Ryotaro Nakamura, MD, City of Hope Medical Center
Julkaisuja ja hyödyllisiä linkkejä
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
- Patologiset prosessit
- Neoplasmat sivustoittain
- Neoplasmat
- Krooninen sairaus
- Sairauden ominaisuudet
- Immuunijärjestelmän sairaudet
- Neoplasmat histologisen tyypin mukaan
- Hematologiset sairaudet
- Lymfaattiset sairaudet
- Lymfoproliferatiiviset häiriöt
- Immunoproliferatiiviset häiriöt
- Leukemia, B-solu
- Lymfooma
- Leukemia, myeloidi
- Luuydinsairaudet
- Leukemia, imusolmukkeet
- Leukemia
- Myeloproliferatiiviset häiriöt
- Leukemia, myelogeeninen, krooninen, BCR-ABL-positiivinen
- Patologiset tilat, merkit ja oireet
- Hemic- ja imusuutteet
- Hematologiset kasvaimet
- Leukemia, lymfosyyttinen, krooninen, B-solu
- Lymfooma, non-Hodgkin
- Myelodysplastiset oireyhtymät
- Myelodysplastiset-myeloproliferatiiviset sairaudet
- Hodgkinin tauti
- Primaarinen myelofibroosi
- Leukemia, myelooinen, krooninen vaihe
- Leukemia, myelooinen, kiihtynyt vaihe
Muut tutkimustunnusnumerot
- 18007
- 18007 (Muu tunniste: City of Hope Medical Center)
- NCI-2018-01115 (Rekisterin tunniste: CTRP (Clinical Trial Reporting Program))
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