ImmunityBio Inc. ( IBRX ) presented two indirect treatment comparison analyses, highlighting efficacy and safety outcomes for ANKTIVA plus Bacillus Calmette-Guérin (BCG) in patients with BCG-unresponsive non-muscle invasive bladder cancer with carcinoma in situ, with or without papillary disease.
The presentations compared ANKTIVA (nogapendekin alfa inbakicept-pmln) combined with BCG against two FDA-approved therapies — Ferring Pharmaceuticals’ Adstiladrin (nadofaragene firadenovec-vncg) and Johnson & Johnson’s INLEXZO (TAR-200).
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In one matching-adjusted indirect comparison, ImmunityBio ( IBRX ) evaluated data from the QUILT-3.032 study against results from the trial involving nadofaragene firadenovec-vncg.
The ANKTIVA plus BCG regimen produced an anytime complete response rate of 69.7%, compared with 53.4% for nadofaragene firadenovec-vncg.
The company also reported a median complete response duration of 22.1 months for the ANKTIVA combination versus 9.7 months for the comparator therapy.
In addition, cystectomy-free survival favored the ANKTIVA regimen, while overall survival differences between the treatments were not statistically significant.
A separate matching-adjusted indirect comparison evaluated ANKTIVA plus BCG against TAR-200 using data from the SunRISe-1 trial.
The analysis found that the ANKTIVA regimen achieved a 12-month complete response rate of 49.2%, compared with 45.9% for TAR-200, although the difference was not statistically significant.
However, patients receiving ANKTIVA plus BCG experienced fewer treatment-related adverse events. The study reported treatment-related adverse events in 61.7% of patients receiving the ANKTIVA regimen versus 83.5% for TAR-200.
According to the company, the analysis showed a statistically significant 68% reduction in the odds of treatment-related adverse events for patients treated with ANKTIVA plus BCG.
IBRX Price Action: ImmunityBio ( IBRX ) shares were down 3.94% at $7.97 at the time of publication on Tuesday, according to Benzinga Pro data.
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