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Efficacy of oncolytic adenovirus injection combined with programmed death receptor (PD-1) inhibitors in the treatment of advanced solid tumors: a multicenter, prospective, case registration study

Efficacy of oncolytic adenovirus injection combined with programmed death receptor (PD-1) inhibitors in the treatment of advanced solid tumors: a multicenter, prospective, case registration study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067289
Enrollment
Unknown
Registered
2023-01-03
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

advanced solid tumors

Interventions

case series:Recombinant human adenovirus type 5 combined with PD-1 injection

Sponsors

Fuzhou First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years (including the boundary value), no gender limit. 2. Patients with confirmed advanced solid tumors, advanced solid tumors that have failed standard treatment or lack of effective treatment. 3. Patients or their legal representatives understand and sign the informed consent form. 4. At least one lesion that can be safely injected intratumorally with oncolytic adenovirus as the target lesion, with a diameter of >=1cm on spiral CT or >=2cm on ordinary CT, and can be measured by imaging. 5. The ECOG score is 0-2.

Exclusion criteria

Exclusion criteria: 1. Physicians participating in the disease registration study believe that patients may not be able to provide continuous follow-up information. 2. Any uncontrollable clinical problems (such as severe psychiatric, neurological, cardiovascular, respiratory or other systemic disease). 3. Contraindications of related drugs (such as oncolytic adenovirus, PD-1 inhibitor, etc.).

Design outcomes

Primary

MeasureTime frame
Objective Response Rate(ORR);Disease Control Rate(DCR);

Secondary

MeasureTime frame
Progression Free Survival(PFS);Overall Survival(OS);

Countries

China

Contacts

Public ContactXie Fangwei

Fuzhou First Hospital

9714497@qq.com+86 135 0935 6590

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026