On October 14, the U.S. Food and Drug Administration announced that Anktiva (nogapendekin alfa inbakicept-pmln), used ...
A study of 180 bladder tumors finds that survival drops only when the high-grade component exceeds 27.5 percent, far above ...
ImmunityBio (IBRX) stock fell 7.25% to $9.27 despite ANKTIVA trial results showing a 71% response rate and lasting benefits ...
FDA approved the drug Anktiva for adults with high-grade papillary-only non-muscle invasive bladder cancer that has not ...
The decision gives certain patients whose cancer has resisted BCG therapy another treatment option aimed at preserving the bladder. Here’s who qualifies and what the evidence shows.
Anktiva is now approved for BCG-unresponsive papillary-only bladder cancer. Here’s what the bladder-sparing option involves, ...
On October 14, 2026, the FDA expanded the approved use of Anktiva (nogapendekin alfa inbakicept-pmln), given with Bacillus Calmette-Guérin (BCG), to include adults with high-grad ...
Researchers developed a urine test that detects bladder cancer, predicts which patients will benefit from immunotherapy ...
The US Food and Drug Administration recently approved an alternative treatment option for patients with BCG-unresponsive high ...
The FDA expanded approval of Anktiva for bladder cancer. The agent is the first approved treatment for BCG-unresponsive, high ...
In October 2026, CG Oncology appointed Isabel Kalofonos as Chief Commercial Officer, tasking her with leading commercial ...
The Food and Drug Administration has expanded its approved indication for ImmunityBio's Anktiva, a bladder-cancer treatment. The new indication expands Anktiva to be used in combination with Bacillus ...