CLAIM #37125 · Eli Lilly and Company (LLY) · 2026Q1 earnings call · Apr 30, 2026 · due Dec 31, 2026
“And we plan to submit the results of BRUIN CLL-322 to regulators later this year.”
Dr. Dan Skovronsky · Chief Scientific and Product Officer
How to check this claim
Look at: Regulatory submission of BRUIN CLL-322 trial results (e.g., NDA/sNDA/sBLA or equivalent filing) to a regulatory agency
It came true if: Company or regulator confirms a regulatory submission based on BRUIN CLL-322 data was made by 2026-12-31
Where: Company press releases, regulatory agency filing announcements (FDA/EMA), or management commentary on subsequent earnings calls
In context
“on regimen and was the first medicine to utilize and outperform a venetoclax control containing control arm in a Phase III in the history of CLL drug development. As shown on Slide 17, Petabit has now been successful in 4 Phase III studies in CLL, each with compelling efficacy and profitability. [indiscernible] has been studied across early and later line settings of CLL, demonstrated efficacy as a monotherapy and in combination and showed efficacy head-to-head against chemo immunotherapy, a covalent BTK inhibitor and now a venetoclax-based regimen. The breadth of evidence suggests pertibritnib has potential to become a foundational therapy in CLL. SeafromBrewen CLL-313 and Brewin CLL14 and are currently under review by regulators for potential label expansion into the first-line setting. And we plan to submit the results of BRUIN CLL-322 to regulators later this year. Building on the Breakthrough Therapy Designation received gene for platinum-resistant ovarian cancer, we initiated second Phase III trial, both [indiscernible] our fully receptor alpha in about drilling conjugate to platinum-sensitive ovarian cancer. We also announced the acquisition of Colonia Therapeutics, Colonial's lentiviral in vivo CAR T platform they show very promising early clinical results in people with multiple myeloma, and we look forward to rapidly advancing the lead program in the [indiscernible] team as well as building future medicines using this technology platform. Earlier this week, we announced the acquisition of Ajax Therapeutics, the lead program, the Phase I JAK2 inhibitor for myelofibrosis and polycythemia vera builds on Lilly's established capabilities in blood c”
Verify independently
SEC filings for LLY ↗ · Claim quote is verbatim from the 2026Q1 earnings call.