Clinical trial · Interventional
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
NCT07581704CI-TRIAL-00113539recruitingPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a single center, single arm Phase Ib study with expansion cohort designed to establish the safety and physiologic effects of sirolimus pre-conditioning followed by T-cell engaging bispecific antibody therapy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Sirolimus | Drug | Sirolimus | ALIAS |
| Talquetamb | Biological | — | UNRESOLVED |
| Teclistamab | Biological | Teclistamab | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Sirolimus in combination with teclistamab or talquetamab
- description
- 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.
- interventionNames
- Drug: Sirolimus
- Biological: Teclistamab
- Biological: Talquetamb
Primary outcomes (2)
- measure
- Phase Ib: Dose limiting toxicities (DLTs) as measured by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
- timeFrame
- From treatment initiation through 30 days post last dose of study treatment
- description
- 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.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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.
1. Anti-BCMA x CD3 bispecific antibody (for example: teclistamab, elranatamab)
2. Anti-GPRC5d x CD3 bispecific antibody (for example: talquetamab)
3. Anti-GPRC5d x CD3 x CD38 trispecific antibody
4. Anti-BCMA x CD3 x CD38 trispecific antibody
5. Anti-BCMA x CD3 x GPRC5d trispecific antibody
6. Anti-BCMA chimeric antigen T-cell (for example: idecabtagene vicleucel, ciltacabtagene autoleucel)
7. 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).References
Publications (0)
Data not yet available
No reference posted for this study.