ClinicalTrials.Veeva

Menu

Autologous and Allogeneic Whole Cell Cancer Vaccine for Metastatic Tumors

H

Hadassah Medical Center

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Breast Cancer
Melanoma
Gastric Cancer
Kidney Cancer
Lung Cancer
Ovarian Cancer
Colorectal Cancer

Treatments

Biological: Autologous or Allogeneic tumor cells

Study type

Interventional

Funder types

Other

Identifiers

NCT00722228
0359-08-HMO-CTIL

Details and patient eligibility

About

This study is based on the finding that tumor cells that are grown in the laboratory can be modified in such a way that, when injected to the patient, they will stimulate his/her immune response. This approach will be evaluated in patients with melanoma and colorectal, gastric, ovarian, breast, lung and kidney epithelial cancer. Tumor cells grown in the laboratory will be modified to make them stimulatory to the immune system, irradiated to kill them, and injected to the patient eight times at two-week intervals. This protocol is expected to prolong survival of metastatic cancer patients.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • One of the following metastatic cancers: Melanoma, breast, ovary, colorectal, gastric, lung or kidney
  • Above 18 years of age
  • Failure of at least one chemotherapy protocol
  • Clinical performance status of ECOG 0,1
  • Absolute neutrophil count greater than 1000/mm3
  • Serum ALT/AST less than three times the upper limit of normal
  • Serum creatinine less than or equal to 1.6 mg/dl.
  • Must be able to understand and sign the Informed Consent document

Exclusion criteria

  • Below 18 years of age
  • Women who are pregnant
  • Life expectancy of less than three months

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Autologous or Allogeneic tumor cells
Experimental group
Description:
Intervention: 5 vaccine doses, 3 weeks apart, injected subcutaneously.
Treatment:
Biological: Autologous or Allogeneic tumor cells

Trial contacts and locations

1

Loading...

Central trial contact

Hani Steinberg, R.N. B.A.; Tamar Peretz, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems