ChiCTR2600130735 Lisaftoclax Adult Acute Myeloblastic Leukemia Clinical Landscape Report 2026: Design, Endpoints, Sponsor and Readout Outlook
Turn a newly registered trial into a decision-ready clinical landscape. This report examines ChiCTR2600130735 using PatSnap Clinical Trials MCP for protocol design and endpoint evidence, with Drug & Asset MCP and Company & Deal Intelligence MCP used as the companion asset and sponsor enrichment workflow. Explore PatSnap MCP Servers to reproduce the research sequence inside an AI workflow.
MCP evidence snapshot: 1 September 2026. Trial records, recruitment status and projected dates can change after the snapshot and should be rechecked before operational decisions.
Why ChiCTR2600130735 is a hot trial to watch
Adult Acute Myeloblastic Leukemia is being segmented by mechanism, treatment setting, geography and endpoint architecture. ChiCTR2600130735 is notable because it evaluates Lisaftoclax in a Phase 2 design sponsored by The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine. The main development question is whether the protocol can translate its rationale into a clinically interpretable and operationally credible readout.
Trial landscape snapshot
| Field | Indexed detail |
|---|---|
| Registration | ChiCTR2600130735 |
| Official title | Study of Mitoxantrone, Cytarabine and Lisaftoclax Combination Therapy for Newly Diagnosed Adult Acute Myeloid Leukemia (MAL-AML II) |
| Phase / status | Phase 2 / Not yet recruiting |
| Intervention | Lisaftoclax |
| Sponsor | The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine |
| Geography | China |
| Enrollment | 60 |
| Primary endpoint | Composite complete remission (CR+CRi) rate after induction cycles |
| Endpoint time frame | Weeks 4–5 after the first and second induction cycle |
| Primary completion / readout proxy | Not reported |
Protocol design and endpoint interpretation
The indexed record describes a Phase 2 study of Lisaftoclax in Adult Acute Myeloblastic Leukemia.
Allocation is not reported, masking is NA, and the intervention model is Single Group Assignment. Planned enrollment of 60 participants across China shapes statistical precision, execution risk and external validity. Interpretation should account for baseline risk, prior therapy, assessment schedule, missing-data handling and clinical relevance—not only statistical significance.
- Composite complete remission (CR+CRi) rate after induction cycles (Weeks 4–5 after the first and second induction cycle) — Metric/method of measurement*Bone marrow aspirate morphology assessment, CR/CRi defined by ELN criteria.
Readout outlook and evidence gap
The current protocol points to Not reported as the best available readout proxy. Because this is an active or newly posted study, a trial-specific result citation is not included until a normalized clinical-trial-result record becomes available. That gap is itself operationally important: teams should monitor first result indexing, conference abstracts, protocol amendments and changes to the primary-completion date.
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Asset and sponsor context
Drug & Asset MCP profile: Lisaftoclax is indexed as No normalized modality returned, with target No normalized target returned, mechanism No normalized mechanism returned, and global highest development status No normalized global status returned.
Company & Deal Intelligence MCP profile: The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine is resolved to a normalized organization record in Guangzhou, China. The organization workflow adds identity, location, portfolio and partnering context where available.
The sponsor profile matters because scientific rationale alone does not determine development value. Manufacturing readiness, portfolio fit, geographic reach, partnering capacity and the ability to fund confirmatory development can determine whether a positive signal becomes a competitive asset.
White space around this program
- Sharper patient selection: prospective biomarker or phenotype definitions that identify who is most likely to benefit.
- Clinically interpretable endpoints: outcomes connecting activity with function, symptoms, survival or treatment burden.
- Comparator relevance: evidence against the most decision-relevant contemporary standard of care.
- Broader external validity: evidence across additional geographies, demographic groups and real-world settings.
- Operational differentiation: a development path that closes the readout gap without sacrificing safety or durability.
What to monitor next
Monitor recruitment, enrollment changes, protocol amendments, endpoint hierarchy, primary-completion timing, first result indexing, asset ownership and sponsor partnerships. A change in endpoint, population or ownership can alter the probability of success before a headline data release.
Bottom line
ChiCTR2600130735 provides a focused lens on Adult Acute Myeloblastic Leukemia development. Its value will be determined by whether Lisaftoclax can convert the current Phase 2 design into evidence that is clinically meaningful, operationally credible and differentiated from competing programs.
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