CTR20262556 DXC-006 Astrocytoma Clinical Landscape Report 2026: Design, Endpoints, Sponsor and Readout Outlook
Turn a newly registered trial into a decision-ready landscape. This focused report examines CTR20262556—评估DXC006在多种实体瘤、血液瘤患者中的有效性、安全性的开放、多中心、单臂、两阶段II期临床研究—using PatSnap Clinical Trials MCP for protocol design and endpoint evidence, Drug & Asset MCP for mechanism and development context, and Company & Deal Intelligence MCP for sponsor background. Explore PatSnap MCP Servers to reproduce the workflow inside an AI research process.
MCP evidence snapshot: 20 July 2026; publication date: 20 July 2026. Trial records can change after the snapshot and should be rechecked before operational decisions.
Why CTR20262556 is a hot trial to watch
Astrocytoma is increasingly segmented by mechanism, biomarker, treatment setting, geography and endpoint architecture. CTR20262556 is notable because it evaluates DXC-006 in a Phase 2 design while 客观有效率（ORR） serves as the main decision variable. The critical question is whether the protocol can convert its rationale into a clinically interpretable and operationally credible readout.
PatSnap Clinical Trials MCP makes protocol fields machine-readable, while the companion asset and organization servers add development-status, target and sponsor context.
Trial landscape snapshot
| Field | Indexed detail |
|---|---|
| Registration | CTR20262556 |
| Official title | 评估DXC006在多种实体瘤、血液瘤患者中的有效性、安全性的开放、多中心、单臂、两阶段II期临床研究 |
| Phase / status | Phase 2 / 进行中 （尚未招募） |
| Intervention | DXC-006, DXC006 |
| Sponsor | Hangzhou DAC Biotechnology Co., Ltd. |
| Collaborators | Not reported |
| Geography | China |
| Enrollment | 200 |
| Primary endpoint | 客观有效率（ORR） |
| Endpoint time frame | 统计分析时间 |
| Primary completion / readout proxy | 2026-07-06 |
Design and endpoint interpretation
The phase label is only the starting point. Allocation is 随机化, masking is 开放, and the intervention model is 单臂试验. Planned enrollment of 200 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.
- Primary: 客观有效率（ORR） (统计分析时间)
- Secondary: 不良事件（AE）及严重不良事件（SAE）发生率及严重程度、异常实验室指标 (试验期间)
- Secondary: PK特征 (统计分析时间)
- Secondary: 免疫原性 (统计分析时间)
- Secondary: 实体瘤依据RECIST 1.1标准； 多发性骨髓瘤依据（IMWG）疗效标准； 脑胶质瘤依据RANO 2.0标准。 评价指标：DCR、VGPR及以上的缓解率； PFS、DOR、OS。 (统计分析时间)
Benchmark readouts in the surrounding field
- A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of RDX-002 on Postprandial Triglycerides in Patients Discontinuing the Glucagon-like Peptide-1 (GLP-1) Agonists, Semaglutide, or Tirzepatide for the Treatment of Obesity (Phase 2): Incremental Postprandial Triglycerides (TG)(Mean) = 43.81 percent change (Standard Deviation, 92.373); Incremental Postprandial Triglycerides (TG)(Mean) = -51.91 percent change (Standard Deviation, 72.293)
- A Phase II Study to Evaluate the Delay in Ovulation Following Oral Levonorgestrel Plus Meloxicam Compared to Placebo in Obese But Normal Menstruating Women (Phase 2): Interval From First Dose to Evidence of Ovulation.(Mean) = 2.67 Number of days (Standard Deviation, 1.53); Interval From First Dose to Evidence of Ovulation.(Mean) = 4.0 Number of days (Standard Deviation, 0)
- A Phase 2, Parallel-Group, Double-Blind Study to Investigate Weight Management With LY3841136 Compared With Placebo in Adult Participants With Obesity or Overweight (Phase 2): Percent Change From Baseline in Body Weight at Week 48(Least Squares Mean) = -0.4 percent change (Standard Error, 0.91); Percent Change From Baseline in Body Weight at Week 48(Least Squares Mean) = -9.4 percent change (Standard Error, 1.60)
These indexed results are contextual benchmarks, not direct head-to-head evidence. Population, treatment line, endpoint definitions, follow-up and analysis sets may differ. Their value is to clarify the type and magnitude of evidence already visible in the competitive landscape.
Build a living trial monitor: connect to PatSnap MCP Servers and track status changes, endpoint revisions, primary-completion dates and newly indexed results without manually reconciling separate databases.
Asset and sponsor context
Drug & Asset context: DXC-006 (Phase 2; CD56 x Top I)
Company & Deal Intelligence context: Hangzhou DAC Biotechnology Co., Ltd. — China — http://www.dacbiotech.com
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 decide 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.
- Sequencing evidence: comparative data after the most 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 probability of success before a headline data release.
Bottom line
CTR20262556 is a focused lens on Astrocytoma development. Its value will be determined by whether DXC-006 can convert the current design into evidence that is clinically meaningful, operationally credible and differentiated from indexed benchmark readouts.
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