ADC Therapeutics (ADCT) shares surged 8.49% to close at $4.60 on Tuesday, riding the wave of encouraging clinical trial data. The biotech company is gearing up for a conference call this morning at 8:00 a.m. EST to discuss the latest developments from its LOTIS-7 trial.
The LOTIS-7 represents a Phase 1b open-label study examining how well ZYNLONTA—ADC Therapeutics’ proprietary antibody-drug conjugate—performs when paired with COLUMVI, Roche’s cancer therapeutic, in treating patients with relapsed or refractory diffuse large B-cell lymphoma. The trial protocol also incorporates two additional combination arms: ZYNLONTA with polatuzumab vedotin and ZYNLONTA with mosunetuzumab.
Clinical Efficacy Data Signals Progress
Results unveiled at the European Hematology Association 2025 Congress this June demonstrate the potential of the combination approach. Among 30 patients evaluated for efficacy, the ZYNLONTA and COLUMVI combination delivered a 93.3% overall response rate, with 86.7% achieving complete response—metrics that underscore the promise of this ADC meta treatment strategy for difficult-to-treat lymphoma cases.
These efficacy figures are noteworthy in the context of ADC Therapeutics’ broader mission to develop antibody-drug conjugates that can address challenging hematologic malignancies where treatment options remain limited.
The views expressed herein are those of the author and do not necessarily reflect those of Nasdaq, Inc.
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ADC Therapeutics Stock Climbs on Promising LOTIS-7 Trial Results
ADC Therapeutics (ADCT) shares surged 8.49% to close at $4.60 on Tuesday, riding the wave of encouraging clinical trial data. The biotech company is gearing up for a conference call this morning at 8:00 a.m. EST to discuss the latest developments from its LOTIS-7 trial.
The LOTIS-7 represents a Phase 1b open-label study examining how well ZYNLONTA—ADC Therapeutics’ proprietary antibody-drug conjugate—performs when paired with COLUMVI, Roche’s cancer therapeutic, in treating patients with relapsed or refractory diffuse large B-cell lymphoma. The trial protocol also incorporates two additional combination arms: ZYNLONTA with polatuzumab vedotin and ZYNLONTA with mosunetuzumab.
Clinical Efficacy Data Signals Progress
Results unveiled at the European Hematology Association 2025 Congress this June demonstrate the potential of the combination approach. Among 30 patients evaluated for efficacy, the ZYNLONTA and COLUMVI combination delivered a 93.3% overall response rate, with 86.7% achieving complete response—metrics that underscore the promise of this ADC meta treatment strategy for difficult-to-treat lymphoma cases.
These efficacy figures are noteworthy in the context of ADC Therapeutics’ broader mission to develop antibody-drug conjugates that can address challenging hematologic malignancies where treatment options remain limited.
The views expressed herein are those of the author and do not necessarily reflect those of Nasdaq, Inc.