BiovaxID (dasiprotimut-T)
/ National Cancer Institute, Accentia
- LARVOL DELTA
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August 27, 2022
Fast Tracking-Vaccine Safety, Efficacy, and Lessons Learned: A Narrative Review.
(PubMed, Vaccines (Basel))
- "Five articles about BiovaxID, THERATOPE, Sipuleucel-T, and AIDSVAX were also reviewed. The previous fast-tracked vaccines were safe and efficacious. The lessons drawn from previous studies highlighted the significance of planning and utilizing global resources during significant outbreaks."
Journal • Review • Infectious Disease • Narcolepsy • Novel Coronavirus Disease • Sleep Disorder
June 19, 2021
Chemotherapy Plus Vaccination to Treat Mantle Cell Lymphoma
(clinicaltrials.gov)
- P2; N=26; Completed; Sponsor: National Cancer Institute (NCI); Trial completion date: Jun 2022 ➔ Jun 2021; Active, not recruiting ➔ Completed
Clinical • Trial completion • Trial completion date • Hematological Malignancies • Lymphoma • Mantle Cell Lymphoma • Oncology • CTCs
June 16, 2021
Chemotherapy Plus Vaccination to Treat Mantle Cell Lymphoma
(clinicaltrials.gov)
- P2; N=26; Active, not recruiting; Sponsor: National Cancer Institute (NCI); Trial completion date: Jun 2021 ➔ Jun 2022
Trial completion date • Hematological Malignancies • Lymphoma • Mantle Cell Lymphoma • Oncology • CTCs
May 14, 2012
Biovest to seek marketing approval in the EU for BiovaxID personalized lymphoma cancer vaccine
(Biovest)
- Biovest plans to file for MAA with EMA for BiovaxID, for the treatment of follicular NHL; Under the EMA centralized procedure, Biovest will simultaneously seek approval for BiovaxID for all EU-member countries; Biovest could receive a decision regarding EU marketing approval for BiovaxID within 12 months after the MAA submission
Anticipated MAA submission • Hematological Malignancies • Non-Hodgkin’s Lymphoma
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