EB-104 in Follicular Lymphoma: NCT07168291 Clinical Landscape Report 2026
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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: 28 September 2026. This strategic research report is not medical, regulatory or investment advice. Trial status and dates can change.
Early Phase 1
Clinical phase
Not yet recruiting
Recruitment status
3
Planned enrollment
2028-12-31
Primary-completion proxy
Executive view
NCT07168291 evaluates EB-104 in Follicular Lymphoma. The disclosed sponsor is First Affiliated Hospital of Xi'an Jiaotong University, the design is Interventional, and the geographic footprint is China. The first listed primary endpoint is Incidence of Treatment-related Adverse Events, assessed over 3 years.
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 NCT07168291 and selected peers. clinical_trial_result_fetch supplied detailed result records from the wider Follicular Lymphoma landscape. Drug & Asset MCP drug_fetch was queried for EB-104, while Company & Deal Intelligence MCP organization_fetch was queried for First Affiliated Hospital of Xi'an Jiaotong University.
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 |
|---|---|---|---|---|---|---|
| NCT07168291 | EB-104 | Early Phase 1 / Not yet recruiting | First Affiliated Hospital of Xi'an Jiaotong University | China | Incidence of Treatment-related Adverse Events 3 years | 2028-12-31 |
| NCT07220187 | Cyclophosphamide | Phase 3 / Not yet recruiting | SWOG | Geography not reported | Progression free survival (PFS) Up to 7 years | 2035-10-01 |
| NCT07215585 | Surovatamig | Phase 3 / Recruiting | AstraZeneca PLC | Canada, South Korea, Hong Kong, Belgium, Japan, China, Turkey, Poland, Brazil, United Kingdom, Australia | SRI - Safety evaluation of R-mini-CHOP × 2 followed by AZD0486: Number of participants with treatment-related adverse e… Up to 1 year | 2030-06-10 |
| NCT07200479 | CT1194D CAR-T Cells(Hematology Hospital of Chinese Academy of Medical Sciences) | Phase 1 / Not yet recruiting | Hematology Hospital of Chinese Academy of Medical Sciences | China | To assess the severity and incidence of DLTs, treatment-related adverse events (TRAE), and adverse events of special in… 12 months after CT1194D infusion | 2027-06-28 |
| NCT07197307 | Loncastuximab tesirine | Phase 2 / Recruiting | Universität Leipzig | Germany | Best overall response rate (BORR) 12 months after the start of study therapy | 2030-04-30 |
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.
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Protocol design and endpoint interpretation
NCT07168291 is a Early Phase 1, not yet recruiting study with 3 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 “3 years.” The retrieved endpoint description is: Therapy-related adverse events will be recorded and assessed according to the National Cancer Institute's Common Terminology Criteria for Adverse Events (CTCAE, Version 5.0) or ASTCT consensus..
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 3 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
5 recent result records were selected as contextual evidence for Follicular Lymphoma. These records do not establish direct evidence for NCT07168291 unless the registration number matches.
A Phase II Study Evaluating the Safety and Efficacy of Glofitamab in Combination With Rituximab (R) Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (CHOP) in Circu…
Phase 2; n=46; End of Treatment Complete Response (EOT CR) Rate = 73.3 Percentage of participants (95% Confidence Interval, 58.06 - 85.40) Source: https://clinicaltrials.gov/ct2/show/results/NCT04980222
A Phase 1b Study Evaluating the Safety, Tolerability and Preliminary Anti-tumor Activity of NT-I7 a Long-acting Human IL-7, Post-Kymriah®, Post-Yescarta®, or Post-Breyanzi® in Sub…
Phase 1; n=17; Any TEAEs = 3 Participants ; Any TEAEs = 2 Participants Source: https://clinicaltrials.gov/ct2/show/results/NCT05075603
Ultralow-Dose Interleukin 10–Expressing Chimeric Antigen Receptor T Cells in Relapsed/Refractory Diffuse Large B-Cell Lymphoma
Phase 1; n=13; CR = 84.6 % Source: https://pubmed.ncbi.nlm.nih.gov/42490071/
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
EB-104 is indexed as T-lymphocyte cell therapy with CD19 x CD22 biology and a global stage of Early Phase 1. The asset profile lists Estrella Biopharma, Inc. as an originator or developer.
First Affiliated Hospital of Xi'an Jiaotong University is indexed in China with the website http://www.dyyy.xjtu.edu.cn. Operates as an educational hospital The record lists 22 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 EB-104 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: NCT07168291
Protocol source: https://clinicaltrials.gov/study/NCT07168291
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: 28 September 2026.
EB-104 in Follicular Lymphoma 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 2028-12-31 the leading decision points.
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