Jefferies Global Healthcare Conference 2026
Logotype for Ascentage Pharma Group International

Ascentage Pharma (6855) Jefferies Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Ascentage Pharma Group International

Jefferies Global Healthcare Conference 2026 summary

11 Jun, 2026

Company progress and pipeline highlights

  • Two novel products commercialized in China, with seven molecules in global clinical trials and over 500 patents issued worldwide.

  • Lead assets include a BCL-2 selective inhibitor (lisaftoclax) and a third-generation PI3K-ABL inhibitor (olverembatinib), both in global Phase III trials.

  • Lisaftoclax is the first BCL-2 inhibitor approved in China, with multiple global registration trials ongoing and strong efficacy in high-risk MDS and AML, including patients who failed prior therapies.

  • Olverembatinib shows robust results in CML and Ph-positive ALL, with high response rates and favorable safety, including in heavily pretreated patients.

  • Pipeline includes MDM2-p53 inhibitor, BTK degrader, EED inhibitor, and PI3K-δ inhibitor, with promising early clinical and preclinical data.

Clinical data and differentiation

  • Lisaftoclax offers a convenient dosing schedule and demonstrates lower infection and drug-drug interaction risks compared to competitors.

  • Olverembatinib achieves high molecular response rates, especially in patients with T315I mutation and compound mutations, and is effective in both CML and Ph-positive ALL.

  • Combination regimens, such as MDM2-p53 inhibitor with lisaftoclax, show chemo-free efficacy in pediatric sarcoma and Ph-positive ALL, with high response rates.

  • Recent ASCO presentations highlighted first-in-class combinations and new data in pediatric and adult oncology indications.

  • Multiple assets are positioned to compete with leading global companies in terms of efficacy and safety.

Commercial and strategic outlook

  • U.S. commercialization preparations underway, including hiring a chief commercial officer and building a launch team, targeting readiness by early 2028.

  • First NDA filings for lead assets expected in the second half of next year, with both compounds on similar timelines.

  • Olverembatinib's global commercialization will be led by Takeda under an option agreement.

  • Commercial team in China to expand to 400, aiming to cover 90% of the market.

  • Open to partnerships for co-development and co-promotion in the U.S. and globally.

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