Melanoma (Skin Cancer)Phase 3SCOPE PlusNCT07815574
iSCIB1+ in Combination With Ipilimumab and Nivolumab as First-Line Treatment for Advanced Unresectable Melanoma
A Phase 3 study testing iSCIB1+ and Nivolumab & Ipilimumab in people with Melanoma (Skin Cancer) and Advanced Melanoma, run by Scancell Ltd at 2 sites in 2 countries.
Trial summary
This Phase 3 clinical trial is evaluating whether adding iSCIB1+, an investigational DNA-based cancer vaccine, to standard immunotherapy with nivolumab and ipilimumab can improve outcomes for people with advanced unresectable melanoma. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Melanoma (Skin Cancer), Advanced Melanoma, Metastatic Melanoma
- What is being tested?
- iSCIB1+ and Nivolumab & Ipilimumab
- Type of treatment
- Vaccines, Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 550 participants
- Where
- 2 sitesin 2 countries
- Study dates
- 1 Dec 2026to 1 Dec 2032
- Phase
- Phase 3
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
5.1.Inclusion Criteria
- Participant has histologically confirmed, unresectable Stage III or Stage IV melanoma as defined by the AJCC (Gershenwald et al., 2017). Participants with a diagnosis of melanoma of unknown primary are eligible.
- Participant is positive for at least one of the following HLA alleles: HLA- with an HLA type of any one of HLA MHC class I: A2, A3, A31, Bw4, B44 and B35.
- Participant has been clinically evaluated, and checkpoint inhibition has been determined to be an appropriate treatment for their advanced disease.
- Participant's BRAF status must be known; participants with BRAF mutation positive disease may be enrolled without BRAF-inhibitor treatment at the discretion of the Study Investigator.
- Participant has at least one measurable lesion per RECIST 1.1 criteria by computed tomography CT scan or MRI.
- Participant is at least 18 years of age.
- Participant has a life expectancy of more than 6 months.
- Participant has an ECOG performance status of 0 or 1.
- Participant has adequate organ function as determined by the following laboratory values: Absolute neutrophil count ≥ 1.5 x 109/L Lymphocyte count ≥0.5 x 109/L Platelet count ≥100 x 109/L Hemoglobin >9 g/dL (> 5.6 mmol/L) Serum creatinine or creatinine clearance ≤1.5x ULN >50 mL/min Serum total bilirubin ≤1.5 x ULN or <3.0 mg/dL if participant has Gilbert's syndrome Serum transaminases, AST and ALT ≤2.5 x ULN or ≤5.0 x ULN if liver metastases present
- Participant must be able and willing to provide written IRB/REC-approved informed consent prior to any study-related procedure.
- Women of childbearing potential must agree to use highly effective contraceptive methods prior to study entry, for the whole duration of study treatment, and for at least 5 months following the last dose or in accordance with the SmPC of the IC SOC CPI (whichever is most conservative). See Appendix D: Guidance on Acceptable Contraceptive Methods for full guidance..
- Women of childbearing potential must have a negative serum pregnancy test at screening and within two days before IMP (or placebo) administration.
- Participant must be willing and able to comply with scheduled visits, treatment plan, laboratory tests and other study procedures.
5.2.Exclusion Criteria
- Participant has a diagnosis of mucosal, ocular or acral melanoma.
- Participant has received prior systemic anti-PD1 treatment for advanced disease.
- Participant has received prior adjuvant treatment, defined as treatment following resection of all detectable disease, within 6 weeks of Day 1 (first dose of IMP).
- Participant has BRAF mutation positive disease with evidence of rapid PD.
- Participant has symptomatic brain metastases or carcinomatous meningitis. Symptomatic brain metastases are defined as brain metastases causing neurological signs or symptoms attributable to intracranial disease and/or requiring corticosteroid therapy for the management of brain metastasis-related symptoms. Participant is expected to require and elect any other form of systemic or localized anticancer therapy while receiving study treatment.
- Participants receive treatment with any investigational product within 28 days (or five half-lives of the treatment concerned if longer than 28 days) prior to Day 1.
- Participant has had a previous or current malignancy within 5 years, with the exception of melanoma and curatively treated local tumors.
- Participant has a concurrent illness/diagnosis which are uncontrolled and/or would preclude study conduct and assessment.
- Participant has NYHA class III or IV heart disease.
- Participant has a history of severe hypersensitivity reaction to treatment with a mAb.
- Participant has an active autoimmune disease or a documented history of autoimmune disease or syndrome that requires systemic steroids or immunosuppressive agents above physiological dosing.
- Received a live vaccine or non-live vaccine (including COVID-19 vaccines) within 7 days prior to first dose of study treatment.
- Participant has received systemic steroids or is receiving any other form of immune suppressant medication above physiological dosing within 7 days of Day 1.
- Participant is positive for HIV-1/2 infection or is positive for HBsAg or HCV antigen consistent with active infection.
- Participant has a known current or recent history (within the last year) of substance abuse including illicit drugs or alcohol to the extent where it would negatively affect compliance with the trial protocol based on Study Investigator's decision.
- Participant has received a solid organ transplant.
- Participant is breastfeeding during the study treatment phase, and for at least five months following the last dose or in accordance with the SmPC of I/N (whichever is most conservative).
Trial locations and contacts
2 sites in 2 countries. Contact the study team or a site near you to ask about taking part.
2 sites in 2 countries
United States1 site
University of Colorado Cancer Center
Aurora, Colorado, 80045
Sapna Patel
About this study
Official title: A Phase 3 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Adaptive Study of iSCIB1+ in Combination With Ipilimumab and Nivolumab as First-Line Treatment for Advanced Unresectable Melanoma
This Phase 3 clinical trial is evaluating whether adding iSCIB1+, an investigational DNA-based cancer vaccine, to standard immunotherapy with nivolumab and ipilimumab can improve outcomes for people with advanced unresectable melanoma.
Participants will be randomly assigned to receive either iSCIB1+ or a placebo, in addition to standard treatment with nivolumab and ipilimumab. Neither participants nor study doctors will know which treatment has been assigned. The study will compare how long participants live without their cancer worsening, overall survival, tumor response, safety, and quality of life.
iSCIB1+ is designed to stimulate the immune system to recognize and attack melanoma cells by targeting proteins commonly found on melanoma tumors. Earlier studies have shown encouraging signs of immune activation and anti-tumor activity when iSCIB1+ was combined with checkpoint inhibitor immunotherapy. This study aims to determine whether adding iSCIB1+ to standard immunotherapy provides additional benefit compared with standard immunotherapy alone
Read the detailed description
This is a multicenter, randomized, double-blind, placebo-controlled Phase 3 study evaluating the efficacy and safety of iSCIB1+ in combination with nivolumab and ipilimumab as first-line treatment for adults with advanced unresectable Stage III or Stage IV melanoma who express specific human leukocyte antigen (HLA) types.
Checkpoint inhibitor therapy has significantly improved outcomes for patients with advanced melanoma; however, many patients still experience disease progression. iSCIB1+ is a DNA-based therapeutic cancer vaccine designed to enhance immune recognition of melanoma-associated antigens and may improve the depth and durability of anti-tumor responses when used alongside checkpoint inhibition.
Approximately 550 participants will be randomized in a 1:1 ratio to receive either:
iSCIB1+ plus nivolumab and ipilimumab, or Placebo plus nivolumab and ipilimumab.
The primary objective is to determine whether the addition of iSCIB1+ improves progression-free survival (PFS) compared with placebo when both are administered in combination with nivolumab and ipilimumab.
Secondary objectives include evaluation of:
Overall survival (OS) Objective response rate (ORR) Duration of response (DoR) Disease control rate (DCR) Safety and tolerability Patient-reported quality of life outcomes
The study will also explore immune and biomarker responses in selected participants to better understand the relationship between vaccine-induced immune responses and clinical outcomes.
Participants will continue to be followed for disease progression, survival, safety, and other outcomes for up to four years after randomization.
- Being tested
- iSCIB1+, Nivolumab & Ipilimumab, Placebo
- Keywords
- Melanoma, advanced melanoma, cancer vaccine, skin cancer
- Medical subject headings
- Melanoma, Skin Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
iSCIB1+Biological
Also called ImmunoBody®
iSCIB1+ is a DNA-based therapeutic cancer vaccine designed to enhance T-cell immune responses against melanoma-associated antigens. The vaccine encodes epitopes derived from glycoprotein 100 (gp100) and tyrosinase-related protein 2 (TRP-2) that are delivered using Scancell's ImmunoBody® platform. In this study, iSCIB1+ is administered by intramuscular injection with electroporation in combination with nivolumab and ipilimumab for the treatment of advanced unresectable melanoma. The intervention is intended to augment anti-tumor immune responses and improve clinical outcomes when added to standard checkpoint inhibitor therapy.
Nivolumab & IpilimumabDrug
Also called Yervoy, BMS-734016, Opdivo, BMS-936558
Nivolumab is a programmed death-1 (PD-1) immune checkpoint inhibitor monoclonal antibody administered according to the protocol-defined treatment regimen. Ipilimumab is a cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) immune checkpoint inhibitor monoclonal antibody administered according to the protocol-defined treatment regimen.
PlaceboOther
Also called Dulbecco's Phosphate-Buffered Saline, D-PBS
The placebo is a Dulbecco's Phosphate-Buffered Saline (D-PBS) solution for intramuscular injection that contains no iSCIB1+ plasmid DNA. It is formulated to be visually and physically indistinguishable from iSCIB1+ and is administered using the same procedures to maintain study blinding. The placebo serves as the comparator in this trial when administered in combination with nivolumab and ipilimumab.
| Study group | Role | What they receive |
|---|---|---|
| iSCIB1+ in combination with Ipilimumab and Nivolumab | Experimental | Participants will receive iSCIB1+ in combination with standard immunotherapy consisting of nivolumab and ipilimumab. Treatment will be administered according to the protocol-defined dosing schedule. Following induction treatment with nivolumab and ipilimumab, participants will continue nivolumab maintenance therapy. This arm is designed to evaluate whether the addition of iSCIB1+ improves clinical outcomes compared with placebo when administered in combination with nivolumab and ipilimumab in participants with advanced unresectable melanoma. Receives: Biological: iSCIB1+; Drug: Nivolumab & Ipilimumab |
| Placebo + Nivolumab and Ipilimumab | Placebo comparator | Participants will receive placebo in combination with standard immunotherapy consisting of nivolumab and ipilimumab. Treatment will be administered according to the protocol-defined dosing schedule. Following induction treatment with nivolumab and ipilimumab, participants will continue nivolumab maintenance therapy. This arm serves as the comparator for evaluating the efficacy and safety of iSCIB1+ when added to standard first-line immunotherapy in participants with advanced unresectable melanoma. Receives: Drug: Nivolumab & Ipilimumab; Other: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Progression-Free Survival (PFS)
Progression-free survival (PFS), defined as the time from randomization to the earliest occurrence of disease progression per RECIST v1.1 as assessed by Blinded Independent Central Review (BICR) or death from any cause.
Measured: Up to 4 years after randomization.
Secondary outcomes (9)
Overall Survival (OS)
Overall survival, defined as the time from randomization to death from any cause.
Measured: Up to approximately 4 years months after randomization.
Objective Response Rate (ORR)
Objective response rate, defined as the proportion of participants achieving a confirmed complete response (CR) or partial response (PR) according to RECIST v1.1 as assessed by BICR.
Measured: Up to 4 years after randomization.
Duration of Response (DoR)
Duration of response, defined as the time from first documented objective response (CR or PR) until disease progression per RECIST v1.1 or death from any cause.
Measured: Up to 4 years after randomization.
Disease Control Rate (DCR)
Disease control rate, defined as the proportion of participants achieving complete response, partial response, or stable disease according to RECIST v1.1 as assessed by BICR.
Measured: Up to 4 years after randomization.
Incidence of Treatment-Emergent Adverse Events (TEAEs)
Incidence, nature, severity, and relationship of treatment-emergent adverse events, graded according to NCI CTCAE.
Measured: From informed consent and up to 4 years from randomization
Incidence of Serious Adverse Events (SAEs)
Incidence of serious adverse events.
Measured: From informed consent and up to 4 years from randomization
Change from baseline in EORTC QLQ-C30 Global Health Status/Quality of Life score
The EORTC QLQ-C30 Global Health Status/Quality of Life scale ranges from 0 to 100, with higher scores indicating better quality of life.
Measured: From informed consent and up to 4 years from randomization
Change from baseline in EQ-5D-5L Health Utility Index Score
EQ-5D-5L index values are derived from participant responses across five health dimensions.
Measured: From informed consent and up to 4 years from randomization
Number of participants reporting symptomatic adverse events according to PRO-CTCAE items
Participant-reported symptom burden will be assessed using selected PRO-CTCAE symptom items. Individual responses are scored according to the PRO-CTCAE scoring manual.
Measured: From informed consent and up to 4 years from randomization
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Sep 2026
- Study start1 Dec 2026 (estimated)
- Primary completion1 Dec 2028 (estimated)
- Study completion1 Dec 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Melanoma (Skin Cancer)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This study uses a randomized, double-blind, placebo-controlled, parallel-group design. Eligible participants will be assigned in a 1:1 ratio to receive either iSCIB1+ plus nivolumab and ipilimumab or placebo plus nivolumab and ipilimumab. Randomization will be stratified according to protocol-defined factors to ensure balanced treatment groups. The study is designed to evaluate whether the addition of iSCIB1+ to standard first-line immunotherapy improves clinical outcomes in participants with advanced unresectable melanoma. Both participants and study personnel involved in study conduct and assessment will remain blinded to treatment assignment throughout the study, except where unblinding is required for participant safety or other protocol-defined reasons. All participants will receive standard-of-care nivolumab and ipilimumab induction treatment followed by nivolumab maintenance therapy in accordance with the protocol. Efficacy, safety, patient-reported outcomes, survival, and bio
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 550 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Scancell Ltd
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- PPD, Part of Thermo Fisher Scientific, Egeen
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07815574
- Sponsor's protocol ID
- SCIB1-003
- Acronym
- SCOPE Plus
- Status last verified
- Sep 2026
- First submitted
- 3 Sep 2026
- Last updated
- 11 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 3 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Adaptive Study of iSCIB1+ in Combination With Ipilimumab and Nivolumab as First-Line Treatment for Advanced Unresectable Melanoma
- ClinicalTrials.gov ID
- NCT07815574
- Acronym / sponsor ID
- SCOPE Plus / SCIB1-003
- Keywords
- Melanoma, advanced melanoma, cancer vaccine, skin cancer
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 550 participants (estimated)
- Lead sponsor
- Scancell LtdIndustry (pharma, biotech, devices)
- Collaborators
- PPD, Part of Thermo Fisher Scientific, Egeen
- Study start
- 1 Dec 2026 (estimated)
- Primary completion
- 1 Dec 2028 (estimated)
- Study completion
- 1 Dec 2032 (estimated)
- First posted
- 11 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This Phase 3 clinical trial is evaluating whether adding iSCIB1+, an investigational DNA-based cancer vaccine, to standard immunotherapy with nivolumab and ipilimumab can improve outcomes for people with advanced unresectable melanoma.
Participants will be randomly assigned to receive either iSCIB1+ or a placebo, in addition to standard treatment with nivolumab and ipilimumab. Neither participants nor study doctors will know which treatment has been assigned. The study will compare how long participants live without their cancer worsening, overall survival, tumor response, safety, and quality of life.
iSCIB1+ is designed to stimulate the immune system to recognize and attack melanoma cells by targeting proteins commonly found on melanoma tumors. Earlier studies have shown encouraging signs of immune activation and anti-tumor activity when iSCIB1+ was combined with checkpoint inhibitor immunotherapy. This study aims to determine whether adding iSCIB1+ to standard immunotherapy provides additional benefit compared with standard immunotherapy alone
Detailed description
This is a multicenter, randomized, double-blind, placebo-controlled Phase 3 study evaluating the efficacy and safety of iSCIB1+ in combination with nivolumab and ipilimumab as first-line treatment for adults with advanced unresectable Stage III or Stage IV melanoma who express specific human leukocyte antigen (HLA) types.
Checkpoint inhibitor therapy has significantly improved outcomes for patients with advanced melanoma; however, many patients still experience disease progression. iSCIB1+ is a DNA-based therapeutic cancer vaccine designed to enhance immune recognition of melanoma-associated antigens and may improve the depth and durability of anti-tumor responses when used alongside checkpoint inhibition.
Approximately 550 participants will be randomized in a 1:1 ratio to receive either:
iSCIB1+ plus nivolumab and ipilimumab, or Placebo plus nivolumab and ipilimumab.
The primary objective is to determine whether the addition of iSCIB1+ improves progression-free survival (PFS) compared with placebo when both are administered in combination with nivolumab and ipilimumab.
Secondary objectives include evaluation of:
Overall survival (OS) Objective response rate (ORR) Duration of response (DoR) Disease control rate (DCR) Safety and tolerability Patient-reported quality of life outcomes
The study will also explore immune and biomarker responses in selected participants to better understand the relationship between vaccine-induced immune responses and clinical outcomes.
Participants will continue to be followed for disease progression, survival, safety, and other outcomes for up to four years after randomization.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- This study uses a randomized, double-blind, placebo-controlled, parallel-group design. Eligible participants will be assigned in a 1:1 ratio to receive either iSCIB1+ plus nivolumab and ipilimumab or placebo plus nivolumab and ipilimumab. Randomization will be stratified according to protocol-defined factors to ensure balanced treatment groups. The study is designed to evaluate whether the addition of iSCIB1+ to standard first-line immunotherapy improves clinical outcomes in participants with advanced unresectable melanoma. Both participants and study personnel involved in study conduct and assessment will remain blinded to treatment assignment throughout the study, except where unblinding is required for participant safety or other protocol-defined reasons. All participants will receive standard-of-care nivolumab and ipilimumab induction treatment followed by nivolumab maintenance therapy in accordance with the protocol. Efficacy, safety, patient-reported outcomes, survival, and bio
| Arm | Type | Receives |
|---|---|---|
| iSCIB1+ in combination with Ipilimumab and Nivolumab | Experimental | Biological: iSCIB1+, Drug: Nivolumab & IpilimumabParticipants will receive iSCIB1+ in combination with standard immunotherapy consisting of nivolumab and ipilimumab. Treatment will be administered according to the protocol-defined dosing schedule. Following induction treatment with nivolumab and ipilimumab, participants will continue nivolumab maintenance therapy. This arm is designed to evaluate whether the addition of iSCIB1+ improves clinical outcomes compared with placebo when administered in combination with nivolumab and ipilimumab in participants with advanced unresectable melanoma. |
| Placebo + Nivolumab and Ipilimumab | Placebo comparator | Drug: Nivolumab & Ipilimumab, Other: PlaceboParticipants will receive placebo in combination with standard immunotherapy consisting of nivolumab and ipilimumab. Treatment will be administered according to the protocol-defined dosing schedule. Following induction treatment with nivolumab and ipilimumab, participants will continue nivolumab maintenance therapy. This arm serves as the comparator for evaluating the efficacy and safety of iSCIB1+ when added to standard first-line immunotherapy in participants with advanced unresectable melanoma. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| iSCIB1+Also: ImmunoBody®iSCIB1+ is a DNA-based therapeutic cancer vaccine designed to enhance T-cell immune responses against melanoma-associated antigens. The vaccine encodes epitopes derived from glycoprotein 100 (gp100) and tyrosinase-related protein 2 (TRP-2) that are delivered using Scancell's ImmunoBody® platform. In this study, iSCIB1+ is administered by intramuscular injection with electroporation in combination with nivolumab and ipilimumab for the treatment of advanced unresectable melanoma. The intervention is intended to augment anti-tumor immune responses and improve clinical outcomes when added to standard checkpoint inhibitor therapy. | Biological | iSCIB1+ in combination with Ipilimumab and Nivolumab |
| Nivolumab & IpilimumabAlso: Yervoy, BMS-734016, Opdivo, BMS-936558Nivolumab is a programmed death-1 (PD-1) immune checkpoint inhibitor monoclonal antibody administered according to the protocol-defined treatment regimen. Ipilimumab is a cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) immune checkpoint inhibitor monoclonal antibody administered according to the protocol-defined treatment regimen. | Drug | Placebo + Nivolumab and Ipilimumab, iSCIB1+ in combination with Ipilimumab and Nivolumab |
| PlaceboAlso: Dulbecco's Phosphate-Buffered Saline, D-PBSThe placebo is a Dulbecco's Phosphate-Buffered Saline (D-PBS) solution for intramuscular injection that contains no iSCIB1+ plasmid DNA. It is formulated to be visually and physically indistinguishable from iSCIB1+ and is administered using the same procedures to maintain study blinding. The placebo serves as the comparator in this trial when administered in combination with nivolumab and ipilimumab. | Other | Placebo + Nivolumab and Ipilimumab |
Primary outcome
Progression-Free Survival (PFS)
Time frame: Up to 4 years after randomization.
Progression-free survival (PFS), defined as the time from randomization to the earliest occurrence of disease progression per RECIST v1.1 as assessed by Blinded Independent Central Review (BICR) or death from any cause.
9 secondary outcomes
Overall Survival (OS)
Time frame: Up to approximately 4 years months after randomization.
Objective Response Rate (ORR)
Time frame: Up to 4 years after randomization.
Duration of Response (DoR)
Time frame: Up to 4 years after randomization.
Disease Control Rate (DCR)
Time frame: Up to 4 years after randomization.
Incidence of Treatment-Emergent Adverse Events (TEAEs)
Time frame: From informed consent and up to 4 years from randomization
Incidence of Serious Adverse Events (SAEs)
Time frame: From informed consent and up to 4 years from randomization
Change from baseline in EORTC QLQ-C30 Global Health Status/Quality of Life score
Time frame: From informed consent and up to 4 years from randomization
Change from baseline in EQ-5D-5L Health Utility Index Score
Time frame: From informed consent and up to 4 years from randomization
Number of participants reporting symptomatic adverse events according to PRO-CTCAE items
Time frame: From informed consent and up to 4 years from randomization
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing iSCIB1+ and Nivolumab & Ipilimumab in people with Melanoma (Skin Cancer) and Advanced Melanoma, run by Scancell Ltd at 2 sites in 2 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 11 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States, United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Joe Thornton (44 (0) 1865 582 066, joethornton@scancell.co.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Progression-Free Survival (PFS) (time frame: Up to 4 years after randomization.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2026; AzTrials last refreshed its copy on 7 Nov 2026.