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9d
SIDNEY: A Novel Vaccine (EO2463) as Monotherapy and in Combination, for Treatment of Patients With Indolent Non-Hodgkin Lymphoma (clinicaltrials.gov)
P1/2, N=60, Recruiting, Enterome | Trial completion date: Sep 2029 --> May 2032 | Trial primary completion date: Jun 2025 --> May 2026
Trial completion date • Trial primary completion date • Combination therapy
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Rituxan (rituximab) • lenalidomide • EO2463
9ms
Trial primary completion date • Combination therapy
|
Rituxan (rituximab) • lenalidomide • EO2463
over2years
A MULTICENTER PHASE 1/2 TRIAL OF EO2463, A MICROBIAL-DERIVED PEPTIDE THERAPEUTIC VACCINE, AS MONOTHERAPY AND IN COMBINATION WITH LENALIDOMIDE AND RITUXIMAB, FOR TREATMENT OF PATIENTS WITH INDOLENT NHL (EHA 2022)
Results The safety lead-in dose-finding is currently ongoing, and no safety concerns have been observed thus far. Conclusion This is a first in human clinical trial to evaluate safety, determine the recommended phase 2 dose and estimate efficacy of a novel microbial-derived peptide therapeutic vaccine, EO2463, in patients with indolent non-hodgkin lymphoma as monotherapy and in combination with lenalidomide and rituximab.
Clinical • P1/2 data • Combination therapy
|
CD20 (Membrane Spanning 4-Domains A1) • CD8 (cluster of differentiation 8) • TERT (Telomerase Reverse Transcriptase) • CD22 (CD22 Molecule) • CD4 (CD4 Molecule) • CD68 (CD68 Molecule) • TNFRSF13C (TNF Receptor Superfamily Member 13C)
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Rituxan (rituximab) • lenalidomide • EO2463
over3years
Clinical • New P1/2 trial • Combination therapy
|
IFNG (Interferon, gamma) • CD22 (CD22 Molecule) • PIAS4 (Protein Inhibitor Of Activated STAT 4)
|
Rituxan (rituximab) • lenalidomide • EO2463
over3years
Clinical • Enrollment open • Combination therapy
|
IFNG (Interferon, gamma)
|
Rituxan (rituximab) • lenalidomide • EO2463
4years
Clinical • New P1/2 trial • Combination therapy
|
IFNG (Interferon, gamma)
|
Rituxan (rituximab) • lenalidomide • EO2463