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NIZ985 + Spartalizumab for Solid Cancers
Phase 1
Waitlist Available
Research Sponsored by Novartis Pharmaceuticals
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a new drug, NIZ985, alone and with two other drugs, in patients with advanced cancers that have worsened after previous treatments. The treatment works by enhancing the immune system's ability to fight cancer.
Who is the study for?
This trial is for adults with advanced solid tumors or lymphoma, including melanoma and non-small cell lung cancer (NSCLC), who've had standard treatments fail. They should be in good physical condition, have measurable disease, and be able to follow the study rules. People can't join if they're on high-dose steroids, have other active cancers or serious heart conditions, recently received certain therapies or live vaccines, are pregnant/nursing, or have severe allergies to study drug ingredients.
What is being tested?
The trial is testing NIZ985 alone and combined with Spartalizumab or Tislelizumab to find safe doses and schedules. It aims to understand how these drugs affect the body (pharmacokinetics) and their preliminary effects on tumor growth.
What are the potential side effects?
Potential side effects may include reactions at the infusion site, immune system-related issues affecting various organs due to increased activity of white blood cells (IL-15 stimulation), fatigue, nausea, as well as risks associated with biopsies.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Dose intensity
Dose interruptions and reductions
Incidence of Dose Limiting Toxcities (DLTs) in escalation and expansion
+1 moreSecondary study objectives
Best Overall Response (BOR)
Disease control Rate (DCR)
Duration of Response (DOR) (expansion groups only)
+4 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Arm 2Experimental Treatment3 Interventions
Combination arm. NIZ985 and Spartalizumab combination is administered starting at Cycle 1 Day 1 in dose escalation. NIZ985 and tislelizumab combination is administered starting at Cycle 1 Day 1 in dose expansion.
Group II: Arm 1Experimental Treatment2 Interventions
Single agent arm. NIZ985 is administered as a single agent (subjects may be treated with the NIZ985-Spartalizumab combination after their first disease re-evaluation)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Spartalizumab
2017
Completed Phase 3
~840
Tislelizumab
2018
Completed Phase 3
~4700
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Non-Small Cell Lung Cancer (NSCLC) and Melanoma include immune checkpoint inhibitors like PD-1, PD-L1, and CTLA-4 inhibitors. These treatments, such as spartalizumab and tislelizumab, work by blocking proteins that suppress the immune system, thereby enhancing the body's ability to attack cancer cells.
This mechanism is crucial for NSCLC and Melanoma patients as it helps the immune system recognize and destroy cancer cells that typically evade immune detection, potentially leading to improved tumor control and survival rates.
Chemotherapy for advanced non-small cell lung cancer in the elderly population.Chemotherapy for advanced non-small cell lung cancer in the elderly population.
Chemotherapy for advanced non-small cell lung cancer in the elderly population.Chemotherapy for advanced non-small cell lung cancer in the elderly population.
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Who is running the clinical trial?
Novartis PharmaceuticalsLead Sponsor
2,904 Previous Clinical Trials
4,207,955 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are able to perform daily activities without being limited by your health, and the doctor thinks you can complete at least 28 days of treatment.You have a heart problem that affects your health.You have another type of cancer that is getting worse or needs treatment.You are taking high doses of steroids or other medications that weaken your immune system, except for replacement steroids for adrenal insufficiency, within 7 days of starting the study treatment.You have an active HIV, HBV, or HCV infection.You have a serious infection that needs strong antibiotics.You currently have an autoimmune disease that is known or suspected.You have received radiation therapy within 2 weeks before starting the study drug.You have been treated with certain types of immunotherapy in the past, and it worked for a while but then stopped working.You have had a specific type of skin cancer called melanoma, and have been treated with certain medications in the past that target the immune system, and your cancer responded and then started growing again.You have advanced solid tumors or lymphoma that have not responded to standard treatments, and there are no other suitable treatments available.You have advanced lung cancer that cannot be removed with surgery and have received up to two previous treatments, one of which was a type of immunotherapy.You need to have a place where a small piece of your tumor can be removed for testing, and your doctor must agree that it's safe for you to have this procedure.You have or had a serious lung disease.You have experienced severe side effects from previous cancer treatment, except for nerve damage, hearing problems, and hair loss.You have used certain medications to help with blood counts or have had a blood transfusion within 2 weeks before starting the study treatment.You have been treated with IL-15 before.You have had a serious allergic reaction to any ingredient in the study drug or similar medications.You have a brain tumor.Your disease must be able to be measured using specific guidelines.
Research Study Groups:
This trial has the following groups:- Group 1: Arm 1
- Group 2: Arm 2
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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