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Sirolimus Pre-conditioning on T Cell Activity and T-cell Engaging Bispecific Antibody Efficacy in Multiple Myeloma
Impact of Sirolimus Pre-conditioning on T Cell Activity and T-cell Engaging Bispecific Antibody Efficacy in Multiple Myeloma
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studiecontact
- Naam: Christopher Strouse, MD
- Telefoonnummer: (319) 356-0489
- E-mail: christopher-strouse@uiowa.edu
Studie Locaties
-
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Iowa
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Iowa City, Iowa, Verenigde Staten, 52242
- Werving
- University of Iowa Health Care
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Contact:
- Christopher Strouse, MD
- Telefoonnummer: (319) 356-0489
- E-mail: christopher-strouse@uiowa.edu
-
Contact:
- Christopher Strouse, MD
- Telefoonnummer: 319-356-0489
- E-mail: christopher-strouse@uiowa.edu
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
To be eligible to participate in this study, an individual must meet all of the following criteria:
- Willingness and ability to provide signed and dated informed consent form.
- Stated willingness to comply with all study procedures and availability for the duration of the study.
- Aged 18 years of older.
- Diagnosis with multiple myeloma, per IMWG Consensus Criteria.20
- Planned for treatment with teclistamab, or talquetamab per standard of care, label indications.15
Prior exposure to any of the following types of T-cell engaging therapies.
- Anti-BCMA x CD3 bispecific antibody (for example: teclistamab, elranatamab)
- Anti-GPRC5d x CD3 bispecific antibody (for example: talquetamab)
- Anti-GPRC5d x CD3 x CD38 trispecific antibody
- Anti-BCMA x CD3 x CD38 trispecific antibody
- Anti-BCMA x CD3 x GPRC5d trispecific antibody
- Anti-BCMA chimeric antigen T-cell (for example: idecabtagene vicleucel, ciltacabtagene autoleucel)
- Anti-FcRL5 x CD3 bispecific antibody
- Required clinical laboratory values during screening phase
Hematologic Parameters Hemoglobin ≥7.0 g/dL; Platelets ≥25 x 109/L; Absolute Lymphocyte Count ≥0.2 x 109/L
Chemistries AST/ALT < 5 x the ULN; Total Bilirubin < 3 x the ULN
- Ability to take oral medication and be willing to adhere to the sirolimus pre-conditioning regimen.
- ECOG performance status of 0, 1, or 2 (KPS of >50).
- For males of reproductive potential: use of condoms or other methods to ensure effective contraception with partner per section5.3.
- Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration.
Exclusion Criteria:
An individual who meets any of the following criteria will be excluded from participation in this study:
- Participants whose multiple myeloma is progressing at a rapid pace requiring immediate anti-myeloma therapy per assessment by the principal investigator or enrolling investigator are excluded.
Excluded concomitant medication exposures:
- Exposure to corticosteroids within 1 week of treatment start
- Exposure to calcineurin inhibitor or mTOR inhibitors (tacrolimus, everolimus, temsirolimus, sirolimus)
- Immunomodulatory monoclonal antibodies targeting tumor necrosis factor alpha (e.g. infliximab), interleukin 6 (e.g. siltuximab),
- Janus kinase inhibitors (e.g. ruxolitinib)
- Any other investigational drug within 28 days
- History of allogeneic hematopoietic cell transplantation.
Excluded concurrent medical conditions:
- Active uncontrolled infection within 7 days prior to treatment start
- Uncontrolled thrombotic event within 3 months of treatment start
- Acute myocardial infarction or acute coronary syndrome within 6 months of start of treatment
- Uncontrolled inflammatory bowel disease
- Active hepatitis B virus, hepatitis C virus, or Human Immunodeficiency Virus infection
- Uncontrolled rheumatologic conditions
Use of ACE-inhibitor therapy within 1 week of treatment start
- Patients found to be taking ace-inhibitor therapy during screening can be included if the ace-inhibitor is substituted for an angiotensin receptor blocking agent. (https://drug-interactions.medicine.iu.edu/main-table)
- CYP3A4/p-gp inhibitors and inducers for 7 days prior to sirolimus doses and 7 days after sirolimus doses(see appendix A for list)
- Any other current active malignancy or history of metastatic malignancy that has the potential to interfere with the safety or efficacy assessment of the investigational intervention
- Pregnancy or lactation.
- Known allergic reactions to study agent (sirolimus).
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Sirolimus in combination with teclistamab or talquetamab
This study is designed to test changes in immune cell populations of patients with multiple myeloma exposed to short pre-conditioning with sirolimus prior to teclistamab or talquetamab.
Safety of the combination will also be assessed.
|
Sirolimus is an immunosuppressant drug.
Sirolimus binds to FK binding protein 12 and inhibits mTOR.
This then suppresses T-cell proliferation and inhibits progression from G1 to S phase of the cell cycle.
Andere namen:
Teclistamab is a bispecific antibody that binds the CD3 receptor on T-cells and the B-cell maturation antigen on multiple myeloma cells and healthy B-lineage cells.
Andere namen:
Talquetamab is a bispecific antibody that binds the CD3 receptor on T-cells and the GPRC5d receptor on multiple myeloma cells.
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Phase Ib: Dose limiting toxicities (DLTs) as measured by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Tijdsspanne: From treatment initiation through 30 days post last dose of study treatment
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The incidence of treatment-emergent adverse events will be summarized by system organ class and/or preferred term, type of adverse event, severity (based on NCI CTCAE v5.0) grades), and relation to study treatment.
The most severe grade per participant will be reported.
Adverse events leading to premature discontinuation from the study intervention and serious treatment-emergent adverse events will be presented in tabular form.
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From treatment initiation through 30 days post last dose of study treatment
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Expansion Cohort: Participants change in the Teffector: Texhausted cell ratio
Tijdsspanne: From treatment initiation through 3 months
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Testing the null hypothesis H0: ΔPost-Pre = 0 versus the alternative H1: ΔPost-Pre ≠ 0. Results will be used as preliminary estimates to inform a subsequent larger trial.
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From treatment initiation through 3 months
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Participant change in the following T-cell subsets: T-regulatory; T-Effector Memory (T-EM); T-Effector Memory expressing RA (T-EMRA)
Tijdsspanne: From treatment initiation through 3 months
|
The within participant change in the following T-cell subsets will be estimated: T-regulatory, T-EM, T-EMRA.
Mixed effects regression models will be utilized to estimate changes.
Random effects will be included to account for the longitudinally correlated nature of repeated measurements.
Graphical plots of the estimated mean and associated 95% confidence intervals by time point in the study will be produced.
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From treatment initiation through 3 months
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The proportion of participants with grade 3 or higher CRS
Tijdsspanne: From treatment initiation through 3 months
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The rate of grade ≥3 CRS will be defined as the proportion of participants who develop grade 3 or higher CRS.
The rate of grade ≥3 CRS will be reported as a binomial proportion along with a two-sided 95% confidence interval.
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From treatment initiation through 3 months
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The proportion of participants with grade 3 or highter ICANS
Tijdsspanne: From treatment initiation through 3 months
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The rate of grade ≥3 ICAN will be defined as the proportion of participants who develop grade 3 or higher ICAN.
The rate of grade ≥3 ICAN will be reported as a binomial proportion along with a two-sided 95% confidence interval.
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From treatment initiation through 3 months
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The proportion of participants with a very good partial response (VGPR) or better at 3 months
Tijdsspanne: Three months after the initiation of treatment
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The 3-month response rate will be defined as the proportion of participants with a very good partial response (VGPR) or better at 3 months.
The 3-month response rate will be reported as a binomial proportion along with a two-sided 95% confidence interval.
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Three months after the initiation of treatment
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Christopher Strouse, MD, University of Iowa
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Vaatziekten
- Hart-en vaatziekten
- Neoplasmata
- Ziekten van het immuunsysteem
- Neoplasmata per histologisch type
- Hematologische ziekten
- Lymfoproliferatieve aandoeningen
- Immunoproliferatieve aandoeningen
- Neoplasmata, plasmacel
- Hemostatische aandoeningen
- Paraproteïnemieën
- Bloed eiwit stoornissen
- Hemorragische aandoeningen
- Hemische en lymfatische ziekten
- Multipel myeloom
- Organische chemicaliën
- Macrolides
- Lactonen
- Sirolimus
Andere studie-ID-nummers
- 202601163
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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