Combination Therapy With GEN0101 and Pembrolizmub in Advanced Melanoma Patients PIb/PII

Inclusion Criteria: Patient will be eligible for this trial if all the following apply:

1. Patient has given written informed consent by themselves

2. Patient aged 20 to 85 years at the time of informed consent

3. Patient has histologically- or cytologically-confirmed melanoma

4. Patient with a diagnosis of incurable and unresectable, Stage IIIC, IIID or Stage IVadvanced melanoma, showing confirmed SD or unconfirmed PD over 12-week treatment withan anti-PD-1 antibody such as nivolumab or Pembrolizumab. To be assigned a status ofSD, changes in tumor measurements must be confirmed by consecutive repeat evaluationsthat should be performed in 4 to 6 weeks after the criteria for response are first metover 12-week of an anti-PD-1 antibody treatment.

5. Patient has a measurable tumor

6. Patient has life expectancy of at least 12 weeks after the first dose ofinvestigational product

7. Patient has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1at screening

8. Patient has met the following criteria of clinical laboratory tests at screening (1)White blood cell (WBC) count over 3,000/μL and neutrophil count over 1,500/μL (2)Platelet count over over 75,000/μL (3)Hemoglobin over 8.0 g/dL (4)AST and ALT ≤ 2.5 × upper limit of normal (ULN) (5)Total bilirubin ≤ 2 × ULN (6)Serum creatinine ≤ 2 ×ULN

9. LDH is not higher than the 2-fold of the upper limit of the institutional reference.

10. A female patient of childbearing potential (a premenopausal woman, a woman withmedically or drug-induced amenorrhea, and a woman with no history of sterilization),who has agreed to use appropriate contraception, e.g., the barrier method and a totalabstinence, during the trial treatment until 3 months passed after completion of thetrial treatment. A male patient who has agreed to use appropriate contraception, e.g.,the barrier method and a total abstinence, during the above period.

Exclusion Criteria: Patient will be excluded from participation if any of the following apply:

1. Patient has brain metastases. Patients with previously treated brain metastases mayparticipate provided they are radiologically stable, i.e. without evidence ofprogression for at least 4 weeks by repeat imaging* (note that the repeat imagingshould be performed during study screening), clinically stable and without requirementof steroid treatment for at least 14 days prior to first dose of study treatment.

2. Patient has showed positive reaction in a prick testing for GEN0101

3. A patient who has the mutant BRAF gene in a tumor biopsy.

4. A patient who has current pneumonitis.

5. Patient concurrently has an active infection requiring systemic therapy.

6. Patient has received other systemic anticancer therapy than an anti-PD-1 antibodytherapy such as nivolumab, Pembrolizumab, or local IFN-beta therapy within 3 weeksbefore the time of informed consent (or within 6 weeks before the time of the informedconsent for a patient who received nitrosourea or mitomycin C)

7. Patient has received another unapproved drug other than anti-PD-L1 antibody within 4weeks before the time of informed consent

8. Patient has intraocular (uveal) melanoma

9. Patient has or had another malignant tumor than melanoma. However, this criterion doesnot apply to a patient who has experienced neither recurrence nor metastasis for atleast 5 years at the time of informed consent.

10. Patient has received systemic corticosteroid or systemic immunosuppressant within 1week before the first dose of investigational product. However, this criterion doesnot apply to a patient who has been on long-term (>6-month) treatment at a low dose (equivalent to oral prednisolone under 10 mg/day) or who received prophylacticimmunosuppressant against contrast media allergy.

11. Patient has received a live vaccine within 30 days before registration

12. Patient has enrolled in another clinical trial and received an investigational productwithin 4 months before the first dose of investigational product, or patient hasintended to be enrolled in another clinical trial in parallel with this clinical trial

13. A patient who has an active TB infection.

14. Female patient is pregnant (including one with positive results from a pregnancy testat screening), lactating, or intending to become pregnant during participation in thistrial and before 3 months have passed after completion of this trial. However, thiscriterion does not apply to a patient who will stop lactating (from the date ofinformed consent until 30 days passed after the last treatment). Of note, femalepatients should undergo a beta-HCG test to demonstrate pregnancy status. Male patientwho does not agree to use appropriate contraception such as the barrier method and atotal abstinence during this trial until 3 months passed after the completion of thistrial. (Detailed method is described in 5.7 Contraception)

15. Patient has psychiatric disease considered to be a potential concern from theviewpoints of follow-up and protocol adherence

16. Patient had given autografting or allografting of organ or tissue (receiving animmunosuppressant)

17. Patient has over 10%-shorter prothrombin time (PT) compared to lower limit of normal (LLN) or over 1.5-fold longer activated partial thromboplastin time (APTT) compared toULN at screening

18. Patient has showed positive reaction to any of HBs antigen, HCV antibody, HIV-1antibody, or HIV-2 antibody at screening. However, even if it is positive for HCVantibody, it should not be excluded when HCV RNA test is negative.

19. Patient is considered ineligible for this trial by the investigator or thesub-investigators