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Individualized cancer immunotherapy with neoantigen complex peptide: a clinical trial

Individualized cancer immunotherapy with neoantigen complex peptide: a clinical trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900020883
Enrollment
Unknown
Registered
2019-01-21
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Primary or metastatic melanoma, gastrointestinal tumor, breast cancer, ovarian cancer, pancreatic cancer, lung cancer, at least one lesion can be removed.

Interventions

Case series:Neoantigen complex peptide loaded DCs.

Sponsors

Gansu Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Primary or metastatic melanoma, gastrointestinal tumor, breast cancer, ovarian cancer, pancreatic cancer, lung cancer, at least one lesion can be removed; 2. RECIST 1.1 is the standard for the measurement and evaluation of metastatic disease; 3. Pathological laboratory diagnosis of metastatic carcinoma; 4. All patients were not satisfied with the conventional treatment; 5. Asymptomatic patients with 3 or fewer brain metastases ( 8.0g/dl, CD4+ cell count > 200/L without the support of granulocyte colony stimulating factor; 11. When patients receive the vaccine, they must undergo more than 4 weeks of systematic treatment, and their toxicity must be restored to level 1 or less (except for toxicity such as alopecia areata or vitiligo). Note: the patient may have undergone minor surgery in the past 3 weeks, as long as all toxicity is restored to grade 1 or less; 12. Pre-survival period 6 months; 13. Ability to understand and willingness to sign a written informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women, women of reproductive age must test negative for pregnancy test within 7 days before enrollment; 2. Primary immunodeficiency of any kind (e.g., severe combined immunodeficiency disease); 3. Concomitant opportunistic infection (the experimental treatment evaluated in this protocol depends on the complete immune system). Patients with compromised immunity were less responsive to experimental treatments and more sensitive to their toxicity; 4. Active systemic infection (e.g. requiring anti-ineffective treatment), coagulation disorder or any other active major disease. Patients surveyed by other institutions.

Design outcomes

Primary

MeasureTime frame
Disease free survival;

Secondary

MeasureTime frame
Over survival;Tumor marker;

Countries

China

Contacts

Public ContactXu Xianghong

Gansu Provincial Hospital

inbeing@163.com+86 0931-8281458

Outcome results

None listed

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