Drugs / PHE885
last change May 2025 re-read 3 minutes ago

PHE885

Cell therapy

Developed for
plasma cell myeloma
Investigated by
Novartis Pharmaceuticals

Trials 2

202120222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT04318327 Jul 2020 → Apr 2025 plasma cell myeloma Novartis Pharmaceuticals Terminated No outcome recorded Stop: Business
Phase 21 trial
Phase 2 NCT05172596 Mar 2022 → May 2025 plasma cell myeloma Novartis Pharmaceuticals Terminated No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2021-12-13 Novartis Pharmaceuticals Results Novartis announces T-Charge™, next-generation CAR-T platform with first-in-human data at ASH 2021 novartis.com ↗
Initial efficacy results include 73% complete response rate at month three with dose level two in the YTB323 study in DLBCL and 100% best overall response in the PHE885 study in multiple myeloma 1,2
2021-12-02 Novartis Pharmaceuticals Results Novartis R&D day spotlights attractive growth profile, underpinned by strong in-market brands, 20 potential high value pipeline assets, and technology platforms novartis.com ↗
In first-in-human trials to be presented at ASH 2021, lead candidates YTB323 and PHE885 showed 75% Complete Response in Diffuse Large B-Cell Lymphoma (DLBCL) at three months and 100% Best Overall Response (BOR) in multiple myeloma, respectively.

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as PHE885 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04318327 ↗
1

NCT05172596 ↗

Modality Cell therapy “autologous T cells genetically engineered with a novel B-cell Maturation Antigen (BCMA)-specific chimeric antigen receptor (CAR)” NCT04318327 ↗
Route Other “Infusion” NCT04318327 ↗