GLOBAL RESEARCH ARCHIVE
ADCT - BUY - LOTIS-7 Completes Enrollment; Full Data by YE Could Be a Positive Catalyst
Research evidence excerpt
ADCT - BUY - LOTIS-7 Completes Enrollment; Full Data by YE Could Be a Positive Catalyst
FLASH NOTE
June 30, 2026
Michael Schmidt, Ph.D. michael.schmidt@guggenheimpartners.com ADCT - BUY - LOTIS-7 Completes Enrollment; Full
617 859 4636 Data by YE Could Be a Positive Catalyst
Sarah Bi, Ph.D.
sarah.bi@guggenheimpartners.com
857 350 0123 Key Message: ADCT confirmed this morning that the global Phase 1b LOTIS-7 study
of Zynlonta (loncastuximab teserine, a CD19 ADC) plus glofitamab (CD20 x CD3 bsAb, Paul Jeng, Ph.D.
paul.jeng@guggenheimpartners.com RHHBY) in 2L DLBCL has completed enrollment of the target n=100 pts, consistent
617 859 4618 with prior guidance. Recall, LOTIS-7 last read out interim data in Dec 2025, where for
49 efficacy-evaluable pts with minimum 6mo follow-up at the time, Zynlonta + glofit
Rosy Liao, Ph.D. achieved a compelling ORR of 90% with substantial depth of response at 78% CRs (see rosy.liao@guggenheimpartners.com
617 859 4663 note). The company intends to present full data for the study at a medical congress
this year and submit for publication by year-end in support of NCCN guideline inclusion,
while in tandem assessing a potential path toward regulatory approval. We reiterate
our positive stance on the LOTIS-7 regimen as positioned among the most potent
and effective combinations in the 2L setting for DLBCL and believe it could competeADCT well with newer CD20 bsAb-based regimens, given its CAR-T-like efficacy coupled ADC Therapeutics SA with simpler administration logistics. For the upcoming readout, we expect heightened Sector: Biotechnology
investor scrutiny on safety, where we think a Gr. 5 TEAE rate <10% (which would be
Company Update on-par with other r/r DLBCL regimens) in conjunction with Breyanzi-like 65%+ CR rate
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