A Study to Evaluate the Safety of Intuvax Administered Intra-tumorally in Patients With Gastrointestinal Stromal Tumors

Gastrointestinal Stromal Tumor Clinical Trial

— GIST  

Official title:

A Phase I Open-label Study Evaluating Safety and Efficacy of Intratumorally Administered Intuvax in Patients With Progressing Gastrointestinal Stromal Tumors (GIST) During Ongoing Second, Third or Fourth Line Treatment With Tyrosine Kinase Inhibition Therapy. A Prospective Single Armed, Open Label Phase I Safety and Efficacy Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02686944
• Other study ID #: IM-103
• Secondary ID: 2015-002689-22
• Status: Completed
• Phase: Phase 1
• Start date: June 1, 2016
• Est. completion date: May 10, 2019

Study information

• Verified date: July 2019
• Source: Immunicum AB
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is a prospective single armed, open label phase I study. Patients with advanced or metastatic GIST and tumor progression despite ongoing treatment with second, third or fourth line TKI treatment, and with at least one measureable tumor lesion, will be eligible for the study. A maximum of 12 patients will be included in this study. The patients will continue with TKI treatment until the 3 months follow up visit. If further tumor progression TKI will be withdrawn but if stable disease or objective response the patient will continue with TKI until progress. The investigational product Intuvax will be injected into a tumor lesion at two or three treatment occasions; day 1, 14 days (±3 days) after the first vaccination, and 28 days (±3 days) after the second vaccination (patient 7-12 only). Intuvax will be injected in a viable part of the tumor, using ultrasound-guided or CT technique for correct administration.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: May 10, 2019
• Est. primary completion date: May 10, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Be informed of the nature of the study and have provided written informed consent.

2. At least 18 years of age.

3. Diagnosis of GIST (according to modified NIH criteria, 2011) where curative excision is no longer an option, i.e. confirmed unresectable or metastatic GIST, and that has progressed on second, third or fourth line tyrosine kinase inhibitor (TKI) treatment.

4. Radiologically measurable tumor(s), i.e at least 3 cm in longest uni-dimensional diameter as measured by CT

5. Clinical and/or CT verified disease progression despite ongoing second, third or fourth line treatment with a TKI

6. Female who has been post-menopausal for more than one (1) year or female of childbearing potential using a highly efficient method of contraception (i.e. a method with less than 1% failure rate [e.g. sterilization, hormone implants, hormone injections, some intrauterine devices, or vasectomized partner with combined use of condom and/or birth control pills]) during study participation. Female of childbearing potential must have a negative blood pregnancy test at Screening, and if randomized to vaccination a negative blood or urine pregnancy test within one (1) day before each dose of Intuvax, or Male agreeing to use condoms during the study participation or male having a female partner who is using a highly efficient method of contraception as described above during the partner's study participation.

Exclusion Criteria:

1. Performance status > ECOG 2

2. Known major reaction/adverse event in connection with previously made vaccination (e.g. asthma, anaphylaxia or other serious reaction)

3. Known major reaction/adverse event in connection with previous transfusions of blood products

4. Active autoimmune disease requiring treatment with systemic immunosuppressive agents, e.g. inflammatory bowel disease, multiple sclerosis, sarcoidosis, psoriasis, autoimmune hemolytic anemia, rheumatoid arthritis, SLE, vasculitis, Sjögren's syndrome, scleroderma, autoimmune hepatitis, and other rheumatological diseases.

5. Tested positive for HIV

6. Active virus disease (HBV and HCV).

7. Ongoing infection that requires treatment with parenteral antibiotics or antiviral medication

8. Corticosteroid treatment per os exceeding 10mg/day within 7 days prior to the first injection of Intuvax. Inhaled, intranasal and local steroids accepted.

9. Inadequate laboratory parameters, i.e.:

• B-Leukocyte count < 3.0 x109/L

• B-Platelet count < 75 x109/L

• B-Hemoglobin < 100 g/L

• P-Prothrombincomplex (PK) >1.4

• P-APT time outside normal limit

10. Previous organ transplantation

11. Pregnant or lactating women

12. Life expectancy less than 3 months.

13. Investigational treatment (within 28 days) prior to the first injection of Intuvax

14. Known blood dyscrasia (bleeding complication)

15. Prior history of invasive cancer within 5 years before screening, except for adequately treated in situ carcinomas or non melanoma skin cancer

16. History of alcohol or substance abuse

17. patient will not be available for follow up assessments

18. Any other reason that, in the opinion of the investigator, contraindicates that the patient participates in the study.

Related Conditions & MeSH terms

• Gastrointestinal Stromal Tumor
• Gastrointestinal Stromal Tumors

Intervention

Biological:
• Intuvax (ilixadencel)
Therapeutic vaccine: allogeneic, proinflammatory dendritic cells, suspension for intratumoral injection

Locations

Country	Name	City	State
Sweden	Department of Breast and Endocrine Surgery, Section of Endocrine and Sarcoma Surgery, Karolinska University Hospital	Stockholm

Sponsors (1)

Lead Sponsor	Collaborator
Immunicum AB

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in vital signs (heart rate, blood pressure, body temperature)		Up to 12 months after vaccination 1
Primary	Changes in lab parameters (hematology and biochemistry) during the study versus baseline		Up to 12 months after vaccination 1
Primary	Adverse events according to CTCAE v 4.03		Up to 12 months after vaccination 1
Secondary	Tumor response by determining changes (PD, SD, PR, CR) in tumor diameter according to mRECIST	Criteria based on the diameter of the contrast-enhanced portions of the tumor	Every 3 months up to 12 months after vaccination 1
Secondary	Tumor response by determining changes (PD, SD, PR, CR) in tumor diameter according to RECIST 1.1.	Criteria based on the maximal tumor diameter	Every 3 months up to 12 months after vaccination 1
Secondary	Tumor response by determining changes (PD, SD, PR, CR) in tumor diameter according to Choi criteria	Criteria based on unidimensional tumor size and tumor density on contrast-enhanced CT images.	Every 3 months up to 12 months after vaccination 1
Secondary	Progression free survival according to mRECIST	Criteria based on the diameter of the contrast-enhanced portions of the tumor	Up to 12 months after vaccination 1
Secondary	Progression free survival according to RECIST 1.1	Criteria based on the maximal tumor diameter	Up to 12 months after vaccination 1
Secondary	Progression free survival according to Choi criteria	Criteria based on unidimensional tumor size and tumor density on contrast-enhanced CT images.	Up to 12 months after vaccination 1
Secondary	Changes in WHO-ECOG score		Up to 12 months after vaccination 1
Secondary	Levels of autoimmunization parameters	Screening of autoantibodies against nuclear antigens (ANA), including the nuclear antigens SSA, SSB, Sm, RNP, Scl-70, Centromeres and Jo-1	Up to 3 months after vaccination 1
Secondary	Levels of alloimmunization parameters	Screening of alloantibodies against HLA-A, B, C (MHC-class I) and HLA-DR (MHC-class II) antigens	Up to 3 months after vaccination 1