Purpose

The Phase 2 study is a multicenter, open-label study of RP1 to further investigate safety and to estimate the efficacy of RP1 at the RP2D in combination with nivolumab in patients with Stage IIIb-IV unresectable melanoma, microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) solid tumors, non-melanoma skin cancer (NMSC), and non-small cell lung cancer (NSCLC).

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1. - At least one measurable and injectable lesion - Have provided a former tumor pathology specimen or be willing to supply a new tumor sample from a biopsy - Have a predicted life expectancy of ≥ 3 months - Measurable disease, according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 criteria - Subjects with MSI-H or dMMR tumors: has diagnosis of MSI-H or metatstatic dMMR tumor (according to protocol definition) who has progressed on prior anti-PD1/PD-L1 therapy. - Subjects with NMSC: has diagnosis of locally advanced or metastatic NMSC that are not considered treatable by surgery including basal cell carcinoma, cutaneous squamous cell carcinoma, basosquamous carcinoma, Merkel cell carcinoma and other non-melanoma skin cancers (per protocol). Patients must have received 8 weeks of anti-PD1/PD-L1 as their last line of therapy and progressed while on treatment. - Subjects with anti-PD1 failed cutaneous melanoma: has confirmed progressive disease while on anti-PD1 treatment for at least 8 weeks and documented BRAF mutation status - Subjects with anti-PD1 failed NSCLC: must have failed prior treatment, including PD1/PD-L1 directed therapy administered either as monotherapy or in combination with platinum-based chemotherapy or anti-CTLA-4. The most recent treatment given must have included an anti-PD1/PD-L1 directed therapy with radiologic disease progression on or after treatment.

Exclusion Criteria

  • Prior treatment with an oncolytic therapy - History of viral infections according to the protocol - Prior complications with herpes infections - Chronic use of anti-virals - Uncontrolled/untreated brain metastasis - History of interstitial lung disease - History of non-infectious pneumonitis - History of clinically significant cardiovascular disease

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Dose escalation of RP1 by intratumoral (IT) injection in superficial tumors
anti-PD-1 monoclonal antibody
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
Experimental
Dose escalation of RP1 by intratumoral (IT) injection in deep/visceral tumors
Dose escalation of RP1 alone in 3 cohorts with IT injections in superficial tumors
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
Experimental
Dose expansion of RP1 and nivolumab (IV) in superficial tumors
Dose escalation of RP1 alone in 3 cohorts with IT injections in superficial tumors
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo
Experimental
Dose expansion of RP1 and nivolumab (IV) in deep/visceral tumors
Doses of RP1 (IT) in deep/visceral tumors with nivolumab (IV)
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo
Experimental
RP1 (IT) and nivolumab (IV) in melanoma
Doses of RP1 (IT) in superficial or deep tumors with nivolumab (IV) in subjects with melanoma
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo
Experimental
RP1 (IT) and nivolumab (IV) in MSI-H/dMMR solid tumors
Doses of RP1 (IT) in superficial or deep tumors with nivolumab (IV) in subjects with MSI-H or dMMR solid tumors
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo
Experimental
RP1 (IT) and nivolumab (IV) in NMSC
Doses of RP1 (IT) in superficial or deep tumors with nivolumab (IV) in subjects with non-melanoma skin cancer
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo
Experimental
RP1(IT) and nivolumab (IV) in anti-PD1 Failed Cutaneous Melanoma
Doses of RP1 (IT) in superficial or deep tumors with nivolumab (IV) in subjects with cutaneous melanoma who have been previously treated with anti-PD1 therapy
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo
Experimental
RP1(IT) and nivolumab (IV) in anti-PD1/PD-L1 Failed NMSC
Doses of RP1 (IT) in superficial or deep tumors with nivolumab (IV) in subjects with non-melanoma skin cancer who have been previously treated with anti-PD1/PD-L1 therapy
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo
Experimental
RP1(IT) and nivolumab (IV) in anti-PD1/PD-L1 Failed NSCLC
Doses of RP1 (IT) in superficial or deep tumors with nivolumab (IV) in subjects with non small cell lung cancer who have been previously treated with anti-PD1/PD-L1 therapy
  • Biological: RP1
    Genetically modified herpes simplex type 1 virus
  • Biological: nivolumab
    anti-PD-1 monoclonal antibody
    Other names:
    • Opdivo

More Details

Status
Active, not recruiting
Sponsor
Replimune Inc.

Study Contact

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.