Expanded Access Study of Talimogene Laherparepvec for Treatment of Subjects With Unresected Stage IIIB-IVM1c Melanoma

• Status: No longer available
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

The study is a phase 3b, multicenter, open-label, single-arm study designed to provide expanded access of Talimogene Laherparepvec for the treatment of subjects with unresected stage IIIB to IVM1c melanoma. The study will also evaluate the safety and tolerability of Talimogene Laherparepvec.

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Amgen
• Treatments: Talimogene laherparepvec

Criteria

Inclusion Criteria:

1. Provide informed consent prior to initiation of any protocol-specific activities/procedures.

2. Male or female age ≥ 18 years at the time of informed consent.

3. Histologically confirmed diagnosis of melanoma

4. Subject has unresected stage lllB to IVM1c melanoma regardless of prior therapy

5. Subject who is not eligible for or cannot access ongoing talimogene laherparepvec clinical trials 6.Subject does not qualify for, or cannot access, other comparable or satisfactory alternative therapy for stage IIIB to IVM1c melanoma

7. Candidate for intralesional therapy 8. Adequate organ function. 9. ECOG performance status of 0, 1, or 2.

Exclusion Criteria:

1. Clinically active cerebral metastases.

2. Greater than 3 visceral metastases.

3. Bone metastases

4. Primary ocular or mucosal melanoma.

5. History or evidence of symptomatic autoimmune pneumonitis, glomerulonephritis, vasculitis, or other symptomatic autoimmune disease.

6. Active herpetic skin lesions or prior complications of HSV-1 infection (eg, herpetic keratitis or encephalitis)

7. Known to have acute or chronic active hepatitis B or C infection

8. Known to have human immunodeficiency virus infection

9. History of other malignancy within the past 3 years

10. Female subject is pregnant or breast-feeding, or planning to become pregnant during protocol treatment and through 3 months after the last dose of talimogene laherparepvec

11. Female subject of childbearing potential who is unwilling to use acceptable method(s) of effective contraception during protocol treatment and through 3 months after the last dose of talimogene laherparepvec.

12. Subject has known sensitivity to any of the products or components to be administered during dosing.

13. Subject has entered this protocol previously.