BRCA1/2 Mutasyonu Taşıyıcılarında INO 5401 Aşılaması

Sade dilde özet

Bu çalışma, BRCA1 veya BRCA2 gen mutasyonu taşıyan bireylerde INO-5401 adlı DNA temelli aşı ile INO-9012'nin (Cellectra 2000 cihazıyla uygulanan) etkilerini incelemektedir. Çalışmaya, patojenik ya da olası patojenik BRCA1/BRCA2 mutasyonu doğrulanmış; bir gruba invaziv meme, yumurtalık, pankreas veya prostat kanseri (breast, ovarian, pancreatic or prostate cancer) tedavisi tamamlanmış, diğer gruba ise kanser tanısı olmayan 18 yaş ve üzeri bireyler katılabilmektedir. Faz 1 aşamasında yürütülmekte; şu an katılımcı almamakta ancak devam etmektedir (active, not recruiting).

Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.

Deney bilgileri

Faz

Faz 1 (Phase 1)

Durum

Devam ediyor, katılım kapalı

Sponsor

Abramson Cancer Center at Penn Medicine

Müdahale

INO-5401, INO-9012, Cellectra 2000

Başlangıç

20.04.2021

Tahmini bitiş

01.03.2027

Ülkeler

United States

İlgili genler

Merkezler

• Philadelphia, United States

Uygunluk kriterleri

Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.

Cohort A Inclusion Criteria:

1. Signed and dated IRB approved informed consent.
2. Females and males age 18+.
3. Documented carrier of a pathogenic or likely pathogenic mutation in BRCA1 or BRCA2.
4. Diagnosis of invasive breast cancer, invasive ovarian cancer, pancreatic cancer (apart from neuroendocrine) or prostate cancer with completion of adjuvant therapy and no clinical evidence of disease according to standard of care.
5. Minimum of 2 clear sites on the skin to allow for injection.
6. ECOG performance status of 0.
7. Normal ECG or ECG without clinically significant findings and which does not require clinical action.
8. Normal bone marrow, hepatic, and renal function.
9. Females who are post-menopausal only.
10. Male subjects with reproductive potential must be willing to use a condom with female partners of reproductive potential and their female sexual partners should use an additional highly effective method of birth control. This is required from screening through 24 weeks after the last dose of immunotherapy.
11. Able and willing to comply with all study procedures.

Cohort B Inclusion Criteria

1. Signed and dated IRB approved informed consent.
2. Females and males age 18+.
3. Documented carrier of a pathogenic or likely pathogenic mutation in BRCA1 or BRCA2.
4. With or without prior prophylactic (but not therapeutic) mastectomy or salpingo-oophorectomy.
5. Minimum of 2 clear sites on the skin to allow for injection.
6. ECOG performance status of 0.
7. Normal ECG or ECG without clinically significant findings and which does not require clinical action.
8. Normal bone marrow, hepatic, and renal function.
9. Females who are post-menopausal only.
10. Male subjects with reproductive potential must be willing to use a condom with female partners of reproductive potential and their female sexual partners should use an additional highly effective method of birth control. This is required from screening through 24 weeks after the last dose of immunotherapy.
11. Able and willing to comply with all study procedures.

Cohort A Exclusion Criteria

1. Previous treatment with INO-5401 or IL-12 containing therapy, or any other DNA immunotherapy.
2. Prior history of invasive cancer other than those listed above. History of localized superficial non-melanoma skin cancers, melanoma in situ, cervical intraepithelial neoplasia, or breast ductal carcinoma in situ is allowed.
3. Pregnant or breast-feeding subjects.
4. Participation in other studies involving investigational drug(s) within 4 weeks prior to study entry and/or during study participation; continued participation in an observational study is allowed.
5. Cardiac pre-excitation syndromes.
6. Prior major surgery within 4 weeks of first study treatment.
7. Presence of acute or chronic bleeding or clotting disorder that would contraindicate intramuscular injections or use of blood thinners within 2 weeks of first study treatment.
8. Any concurrent condition requiring the continued or anticipated use of systemic steroids or immunosuppressive therapy. All systemic corticosteroids must be discontinued at least 4 weeks prior to first study treatment.
9. History of clinically significant disease or other immunosuppressive disease.
10. HIV infection.
11. Known history of hepatitis B and/or hepatitis C with active viral replication.
12. Receipt of any blood product within 2 weeks before signing ICF.
13. Administration of any vaccine, except influenza vaccine, within 4 weeks of the first study treatment. Administration of influenza vaccine within 2 weeks of first study treatment.
14. Presence of metal implants or implantable medical device within 5 cm of the planned site of injection/EP including a cardioverter-defibrillator (ICD) or pacemaker (to prevent a life-threatening arrhythmia) that is located ipsilateral to the intended deltoid injection site, unless deemed acceptable by a cardiologist.
15. Active drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements.
16. Any illness or condition that in the opinion of the investigator may affect the safety of the subject or the evaluation of any study endpoint.
17. Any other conditions judged by the investigator that would limit the evaluation of the subject.

Cohort B Exclusion Criteria

1. Previous treatment with INO-5401 or IL-12 containing therapy, or any other DNA immunotherapy.
2. Prior history of invasive cancer other than those listed above. History of localized superficial non-melanoma skin cancers, melanoma in situ, cervical intraepithelial neoplasia, or breast ductal carcinoma in situ is allowed.
3. Pregnant or breast-feeding subjects.
4. Participation in other studies involving investigational drug(s) within 4 weeks prior to study entry and/or during study participation; continued participation in an observational study is allowed.
5. Cardiac pre-excitation syndromes.
6. Prior major surgery within 4 weeks of first study treatment.
7. Presence of acute or chronic bleeding or clotting disorder that would contraindicate intramuscular injections or use of blood thinners within 2 weeks of first study treatment.
8. Any concurrent condition requiring the continued or anticipated use of systemic steroids or immunosuppressive therapy. All systemic corticosteroids must be discontinued at least 4 weeks prior to first study treatment.
9. History of clinically significant disease or other immunosuppressive disease.
10. HIV infection.
11. Known history of hepatitis B and/or hepatitis C with active viral replication.
12. Receipt of any blood product within 2 weeks before signing ICF.
13. Administration of any vaccine, except influenza vaccine, within 4 weeks of the first study treatment. Administration of influenza vaccine within 2 weeks of first study treatment.
14. Presence of metal implants or implantable medical device within 5 cm of the planned site of injection/EP including a cardioverter-defibrillator (ICD) or pacemaker (to prevent a life-threatening arrhythmia) that is located ipsilateral to the intended deltoid injection site, unless deemed acceptable by a cardiologist.
15. Active drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements.
16. Any illness or condition that in the opinion of the investigator may affect the safety of the subject or the evaluation of any study endpoint.
17. Any other conditions judged by the investigator that would limit the evaluation of the subject.