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Monoclonal Antibodies
NPX267 for Cancer
Phase 1
Recruiting
Research Sponsored by NextPoint Therapeutics, Inc.
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 from first dose through one year
Awards & highlights
No Placebo-Only Group
Summary
This trial tests NPX267, an antibody drug that helps the immune system fight cancer by targeting a specific marker on cancer cells. It focuses on patients with certain cancers, including a type of lung cancer, to find a safe and effective dose. The study will monitor side effects and check how well the drug works against tumors.
Who is the study for?
This trial is for adults with certain advanced cancers, like lung or breast cancer, that no longer respond to standard treatments. They must be fairly active (ECOG status 0 or 1), have normal organ function, and agree to use effective birth control. People can't join if they're on high-dose steroids for autoimmune diseases, have unstable brain tumors, severe lingering side effects from past cancer treatments (except hair loss or long-term nerve pain/skin color changes), or a history of serious immune-related lung/intestine problems.
What is being tested?
NPX267 is being tested in this study. It's an antibody drug given by IV every three weeks aimed at helping the body's immune system recognize and fight cancer cells expressing HHLA2 protein. The study will determine the right dose and assess how patients handle the treatment regarding safety and tolerability.
What are the potential side effects?
Potential side effects of NPX267 may include reactions related to strengthening the immune system against cancer which could affect various organs leading to inflammation-like symptoms; however, specific side effect profiles will be closely monitored throughout the trial.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from first dose through one year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from first dose through one year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Incidence of dose limiting toxicity
Incidence of treatment-emergent adverse events
Number of subjects with tumor response in tumors expressing B7-H7/HHLA2
Secondary study objectives
Area under the concentration curve (AUC) of NPX267
Half-life in circulation (T1/2) of NPX267
Immunogenicity of NPX267
+1 moreOther study objectives
Change in biomarkers of activity
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: NPX267 TreatmentExperimental Treatment1 Intervention
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
Cancer treatments work through various mechanisms to target and destroy cancer cells. Immunotherapy, like NPX267, enhances the body's immune response against cancer by targeting specific proteins that help tumors evade immune detection.
This is crucial for patients as it can lead to more effective and durable responses. Chemotherapy uses drugs to kill rapidly dividing cells, but it can also affect healthy cells, leading to side effects.
Targeted therapy focuses on specific molecular targets associated with cancer, minimizing damage to normal cells. Radiation therapy uses high-energy particles to damage the DNA of cancer cells, inhibiting their ability to reproduce.
Understanding these mechanisms helps patients and doctors choose the most appropriate treatment based on the cancer type and individual patient factors.
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Who is running the clinical trial?
NextPoint Therapeutics, Inc.Lead Sponsor
1 Previous Clinical Trials
144 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My bone marrow, kidney, and liver are functioning normally.My brain metastases are stable and not causing symptoms.I am fully active or can carry out light work.I have had severe lung or colon inflammation due to immune system reactions.My cancer is one of the listed types and has not responded to standard treatments.I don't have lasting side effects from cancer treatment, except for hair loss, long-term nerve damage, or skin color changes.I take more than 10 mg of prednisone daily for an autoimmune disease.
Research Study Groups:
This trial has the following groups:- Group 1: NPX267 Treatment
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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