Tumor antigen-pulsed autologous dendritic cells (Chang Gung Memorial Hospital) in Advanced Hepatocellular Carcinoma: NCT07726329 Clinical Landscape Report 2026
Explore the PatSnap Life Sciences MCP marketplace
This Clinical Landscape Report was built with PatSnap Life Sciences MCP workflows. Clinical Trials MCP supplies protocol and result records, Drug & Asset MCP adds asset context, and Company & Deal Intelligence MCP resolves sponsor background. Use the same structured MCP building blocks in your research workflow.
Data snapshot: 16 September 2026. This strategic research report is not medical, regulatory or investment advice. Trial status and dates can change.
Phase 2
Clinical phase
Active, not recruiting
Recruitment status
100
Planned enrollment
2028-02-01
Primary-completion proxy
Executive view
NCT07726329 evaluates Tumor antigen-pulsed autologous dendritic cells (Chang Gung Memorial Hospital) in Advanced Hepatocellular Carcinoma. The disclosed sponsor is Chang Gung Memorial Hospital, the design is Interventional, and the geographic footprint is Taiwan Province. The first listed primary endpoint is Incidence of Treatment-Related Adverse Events, assessed over up to 48 months..
The key landscape question is whether this protocol can generate a clinically interpretable signal relative to nearby programs. Phase alone is not a measure of evidence quality. Endpoint relevance, comparator choice, masking, enrollment feasibility, patient selection, country coverage and follow-up must be considered together.
PatSnap MCP Servers make this assessment reproducible by keeping protocol facts, result evidence, asset attributes and sponsor identity in separate structured calls.
How the MCP evidence stack was assembled
Clinical Trials MCP clinical_trial_fetch retrieved the design, outcomes, phase, status, enrollment, sponsor, countries and timing for NCT07726329 and selected peers. clinical_trial_result_fetch supplied detailed result records from the wider Advanced Hepatocellular Carcinoma landscape. Drug & Asset MCP drug_fetch was queried for Tumor antigen-pulsed autologous dendritic cells (Chang Gung Memorial Hospital), while Company & Deal Intelligence MCP organization_fetch was queried for Chang Gung Memorial Hospital.
This separation reduces a common diligence error: treating a registry label, a company description or a result excerpt as if each represented the complete evidence package. Explore the source workflow at the PatSnap MCP marketplace.
Trial landscape table
| Trial | Asset / intervention | Phase / status | Sponsor | Geography | Primary endpoint | Readout proxy |
|---|---|---|---|---|---|---|
| NCT07726329 | Tumor antigen-pulsed autologous dendritic cells (Chang Gung Memorial Hospital) | Phase 2 / Active, not recruiting | Chang Gung Memorial Hospital | Taiwan Province | Incidence of Treatment-Related Adverse Events up to 48 months. | 2028-02-01 |
| NCT07761286 | Sintilimab | Phase 1/2 / Not yet recruiting | CSPC Megalith Biopharmaceutial Co., Ltd. | China | Incidence of Adverse Events (AEs) and Serious Adverse Events (SAEs) Up to 2 years. | 2029-09-30 |
| NCT07749859 | Apatinib Mesylate | Phase 2 / Not yet recruiting | Cancer Hospital Chinese Academy of Medical Sciences | China | Objective Response Rate (ORR) From first dose until disease progression, death, or 24 months, which… | 2028-07-01 |
| NCT07746960 | Anlotinib Dihydrochloride | Early Phase 1 / Active, not recruiting | Nanfang Hospital | China | ORR through study completion.Continuously follow up the patient's subsequ… | 2026-10-31 |
| NCT07738055 | Envafolimab | Not Applicable / Not yet recruiting | Tianjin Medical University Cancer Institute and Hospital | Geography not reported | Surgical conversion rate The conversion rate for the first to third cycles of medication (each… | 2029-01-31 |
The table aligns endpoints, sponsors, phases, geographies and readout proxies. It is descriptive, not a head-to-head efficacy comparison. Differences in population, baseline risk, intervention schedule and follow-up can dominate apparent cross-trial differences.
Reproduce the trial-to-asset workflow with PatSnap MCP
Protocol design and endpoint interpretation
NCT07726329 is a Phase 2, active, not recruiting study with 100 planned participants. Allocation is N/A, masking is None (Open Label), and the intervention model is Single Group Assignment.
The primary endpoint is “Incidence of Treatment-Related Adverse Events” over “up to 48 months..” The retrieved endpoint description is: To evaluate the safety of the treatments by assessing the number of participants with treatment-related adverse events..
Interpretation should test whether the endpoint captures a clinically meaningful change, whether its time horizon matches the proposed biology, and whether treatment discontinuation or missing data can bias the estimate. The planned enrollment of 100 should be assessed against expected effect size, event frequency, multiplicity, subgroup plans and attrition.
No named control drug was returned in the protocol field set. A placebo comparator can strengthen internal efficacy assessment, while an active comparator may better test clinical differentiation. Single-arm and open-label programs require greater weight on objective outcomes, independent assessment and external benchmarks.
Indexed readouts in the surrounding landscape
4 recent result records were selected as contextual evidence for Advanced Hepatocellular Carcinoma. These records do not establish direct evidence for NCT07726329 unless the registration number matches.
A Phase 3 Multicenter, Randomized, Double-blinded, Active-controlled, Clinical Study to Evaluate the Safety and Efficacy of Lenvatinib (E7080/MK-7902) With Pembrolizumab (MK-3475)…
Phase 3; n=480; Progression Free Survival (PFS) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) as Assessed by Blinded Independent Central Review (BICR)(Median): Hazard Ratio (HR) = 0.66(95% CI, 0.51 - 0.84), P-Value = 0.0002; Progression Free Survival (PFS) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) as Assessed by Blinded Independent Central Review (BICR)(Median): Hazard Rat… Source: https://clinicaltrials.gov/ct2/show/results/NCT04246177
Early Detection, Accurate Staging, and Biologic Characterization of HCC With Hybrid 68Ga-PSMA-Dual -Contrast PET/MRI and PET/CT Using Cyclotron-Produced 68Ga
Phase 2; n=52; High PSMA uptake, grade 3 or 4 = 25 HCC Lesions Source: https://clinicaltrials.gov/ct2/show/results/NCT04762888
Addition of ipilimumab to atezolizumab plus bevacizumab in advanced hepatocellular carcinoma (PRODIGE 81-FFCD 2101-TRIPLET HCC): phase 2 results from a randomised, multicentre, op…
Phase 2/3; n=226; Adverse Event: acute renal failure = 3% of patients in the atezolizumab plus bevacizumab group experienced acute renal failure ; Adverse Event: acute renal failure = 3% of patients in the atezolizumab plus bevacizumab group experienced acute renal failure Source: https://pubmed-ncbi-nlm-nih-gov.libproxy1.nus.edu.sg/42330996/
Result fields should be reconciled with the source record before quantitative comparison. Population definitions, analysis sets, dose cohorts, estimands, confidence intervals, rescue therapy and follow-up can materially change the meaning of a numerical endpoint. Clinical Trials MCP supports repeatable refreshes as result records change.
Asset and sponsor context
Tumor antigen-pulsed autologous dendritic cells (Chang Gung Memorial Hospital) is indexed as Therapeutic vaccine with target not reported biology and a global stage of Phase 2. The asset profile lists Chang Gung Memorial Hospital as an originator or developer.
Chang Gung Memorial Hospital is indexed in China with the website http://www.chang-gung.com. Functions as a foundation or endowment The record lists 14 development-stage drug assets.
For execution diligence, monitor sponsor ownership, collaborator additions, site expansion, protocol amendments and enrollment revisions. A change in ownership or geography can alter operational confidence as well as the commercial meaning of a future readout.
Development white space
- Endpoint white space. Determine whether a more patient-relevant outcome, longer durability window or blinded central assessment would resolve uncertainty left by the current endpoint.
- Population white space. Test biomarker-defined, treatment-line or risk-stratified subgroups where effect size and unmet need could be clearer.
- Comparator white space. Identify whether the study can support differentiation against the current standard of care rather than only activity against baseline or placebo.
- Geographic white space. Assess whether the disclosed footprint supports recruitment, regulatory transferability and commercial generalizability.
- Sequencing white space. Clarify whether Tumor antigen-pulsed autologous dendritic cells (Chang Gung Memorial Hospital) is intended for monotherapy, combination, maintenance, rescue or an earlier treatment line.
White space should be framed as an unanswered development question, not merely an unoccupied mechanism label. A credible program closes a measurable clinical uncertainty with a design that can be executed and interpreted.
Strategic implications and next readouts
For sponsors, the endpoint hierarchy, safety window, enrollment pace and protocol amendment history should all support the same target product profile. Advancement criteria should be set before the readout and tied to clinical effect, uncertainty, tolerability and operational feasibility.
For business-development teams, differentiation may come from a sharper population, stronger comparator, more durable benefit, simpler delivery or clearer sequencing role. For investors, the central risk is evidence quality relative to time and capital, not the phase label in isolation.
Track recruitment status, enrollment changes, primary-completion timing, endpoint revisions, new result records, sponsor ownership and collaborator changes. Re-run the PatSnap MCP workflow when a surrogate becomes a clinical outcome, a single-country study expands, the comparator changes or a new result materially shifts the competitive benchmark.
Source trail and bottom line
Anchor trial: NCT07726329
Protocol source: https://clinicaltrials.gov/study/NCT07726329
MCP sources: Clinical Trials MCP (clinical_trial_fetch and clinical_trial_result_fetch); Drug & Asset MCP (drug_fetch); Company & Deal Intelligence MCP (organization_fetch).
Data snapshot: 16 September 2026.
Tumor antigen-pulsed autologous dendritic cells (Chang Gung Memorial Hospital) in Advanced Hepatocellular Carcinoma is best understood through the interaction of protocol design, surrounding readouts, asset context and sponsor execution. The current record makes Incidence of Treatment-Related Adverse Events and 2028-02-01 the leading decision points.
Build and refresh clinical landscape reports with PatSnap MCP
