- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07581704
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
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 1
Contatti e Sedi
Contatto studio
- Nome: Christopher Strouse, MD
- Numero di telefono: (319) 356-0489
- Email: christopher-strouse@uiowa.edu
Luoghi di studio
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Iowa
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Iowa City, Iowa, Stati Uniti, 52242
- Reclutamento
- University of Iowa Health Care
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Contatto:
- Christopher Strouse, MD
- Numero di telefono: (319) 356-0489
- Email: christopher-strouse@uiowa.edu
-
Contatto:
- Christopher Strouse, MD
- Numero di telefono: 319-356-0489
- Email: christopher-strouse@uiowa.edu
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
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).
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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.
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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.
Altri nomi:
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.
Altri nomi:
Talquetamab is a bispecific antibody that binds the CD3 receptor on T-cells and the GPRC5d receptor on multiple myeloma cells.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Phase Ib: Dose limiting toxicities (DLTs) as measured by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Lasso di tempo: 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
Lasso di tempo: 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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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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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)
Lasso di tempo: From treatment initiation through 3 months
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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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Christopher Strouse, MD, University of Iowa
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie vascolari
- Malattia cardiovascolare
- Neoplasie
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Malattie ematologiche
- Malattie linfoproliferative
- Disturbi immunoproliferativi
- Neoplasie, plasmacellule
- Disturbi emostatici
- Paraproteinemie
- Disturbi delle proteine del sangue
- Disturbi emorragici
- Malattie emiche e linfatiche
- Mieloma multiplo
- Prodotti chimici organici
- Macrolidi
- Lattoni
- Sirolimo
Altri numeri di identificazione dello studio
- 202601163
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .