A Phase 2 Study to Assess the Safety and Efficacy of IMO-2125 With 8 mg Ipilimumab in Patients With Metastatic Melanoma

The open-label single-arm Phase 2 study was designed to assess the recommended dose for safety, tolerability, pharmacokinetics (PK), immunogenicity, and efficacy of 8 mg IMO-2125 (tilsotolimod) when administered in combination with ipilimumab.

Inclusion criteria

• Patients must have histologically confirmed metastatic melanoma with measurable, stage III (lymph node or in transit lesions) or stage IVA, IVB, or IVC disease.
• Patients must have symptomatic or radiographic progression during or after treatment with a PD-(L)1 inhibitor administered either as monotherapy or in combination.

• The interval between last PD-(L)1 directed treatment and start of study treatment should be at least 21 days.
• Prior BRAF or MEK inhibitor treatment is not required. However, for patients with known BRAF status:

• Those with BRAF wild type may have had a maximum of two previous systemic regimens for the treatment of melanoma.
• Those with a BRAF mutation may have had a maximum of three previous systemic regimens for the treatment of melanoma.
• Prior ipilimumab is permitted.
• Previous treatment with either a PD-1 inhibitor (for patients enrolling on the IMO-2125 + pembrolizumab combination) or CTLA-4 inhibitor (for patients enrolling on the IMO-2125 + ipilimumab combination if applicable) should not have been accompanied by DLT for which permanent discontinuation is recommended (per USPI).

• Patients with a history of Grade ≥2 gastrointestinal symptoms (e.g., diarrhea, colitis) during prior checkpoint inhibitor treatment should be discussed with the Idera Medical Monitor during the Screening Period before starting study treatment.
• Phase 1 patients must have at least two measurable tumor lesions ≥ 1.0 cm that are accessible to biopsy. Phase 2 patients must have at least one measurable lesion (per RECIST v1.1) which may be the same site that is used for the intratumoral injections.
• Patients must be ≥ 18 years of age.
• Patients must have Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 2.
• Patients must meet the following laboratory criteria:

• Absolute neutrophil count (ANC) ≥ 1.5 x 10^9/L (1500/mm3)
• Platelet count ≥ 75 x 10^9/L (75,000/mm3)
• Hemoglobin ≥ 8.0 g/dL (4.96 mmol/L)
• Serum creatinine ≤ 1.5 x upper limit of normal (ULN) or calculated creatinine clearance ≥ 60 mL/minute
• Aspartate aminotransferase (AST) ≤ 2.5 x ULN; alanine aminotransferase (ALT) ≤ 2.5 x ULN; AST/ALT < 5 x ULN if liver involvement
• Serum bilirubin ≤ 1.5 x ULN, except in patients with Gilbert's Syndrome who must have a total bilirubin < 3 mg/dL
• Women of childbearing potential (WOCBP) and men must agree to use effective contraceptive methods from Screening throughout the study treatment period and until at least 90 days after the last dose of IMO-2125, 3 months after the last dose of ipilimumab or at least 4 months after the last dose of pembrolizumab.
• Patients must have an anticipated life expectancy > 3 months.

Exclusion criteria

• Patients who have received prior therapy with a TLR agonist, excluding topical agents. Patients who have received experimental vaccines or other investigational immune therapies should be discussed with the Medical Monitor to confirm eligibility.
• Patients who have received systemic treatment with IFN-α within the previous 6 months prior to enrolling into this study.
• Patients with known hypersensitivity to any oligodeoxynucleotide.
• Patients with active autoimmune disease requiring disease-modifying therapy.
• Patients requiring concurrent systemic steroid therapy higher than physiologic dose (7.5 mg/day of prednisone).
• Patients with any form of active primary or secondary immunodeficiency.
• Patients with another primary malignancy that has not been in remission for at least 3 years.
• Patients with active systemic infections requiring antibiotics or active hepatitis A, B, or C.
• Patients with a known diagnosis of human immunodeficiency virus (HIV) infection.
• Patients who previously had a severe reaction to treatment with a human antibody.
• Patients with known central nervous system, meningeal, or epidural disease.
• Women who are pregnant or breastfeeding.
• Patients with impaired cardiac function or clinically significant cardiac disease.
• Patients with ocular melanoma.