Imzokitug + Pumitamig for Lung Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new combination of treatments to evaluate their safety and effectiveness for people with advanced lung cancer. Participants will receive either a mix of Imzokitug (a potential new drug), Pumitamig (another potential new drug), and standard chemotherapy, or just Pumitamig with chemotherapy. The goal is to determine which option works better as a first treatment for non-small cell lung cancer that has spread or cannot be removed by surgery. Suitable candidates include those with a confirmed diagnosis of advanced non-small cell lung cancer who have not received previous treatment for their advanced cancer. As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to significant advancements in lung cancer treatment.
Do I have to stop taking my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
A study found that Imzokitug, when combined with other treatments, had a manageable safety profile for patients with advanced lung cancer. While side effects occurred, they were not severe. Research also shows that most patients tolerated Imzokitug well.
For Pumitamig, studies suggest it also had a manageable safety profile. No new safety concerns emerged, and few patients discontinued treatment due to side effects.
Both treatments have been deemed safe enough for further testing and are generally well-tolerated by most patients. However, like any treatment, side effects can occur, so discussing any concerns with a doctor is important.12345Why are researchers excited about this trial's treatments?
Researchers are excited about Imzokitug and Pumitamig for treating lung cancer because these drugs offer a fresh approach compared to traditional treatments like chemotherapy and targeted therapies. Imzokitug is unique due to its novel mechanism of action, which specifically targets and inhibits pathways critical for cancer cell survival, potentially leading to more effective tumor reduction. Pumitamig stands out for its ability to boost the immune system's response against cancer cells, which could enhance the body's natural ability to fight the disease. Together, these treatments could offer a powerful combination that not only targets cancer cells directly but also strengthens the body's defenses, offering new hope for improved outcomes in lung cancer treatment.
What evidence suggests that this trial's treatments could be effective for Non-Small Cell Lung Cancer?
This trial will evaluate the effectiveness of Imzokitug and Pumitamig for treating non-small cell lung cancer (NSCLC) in separate treatment arms. Studies have shown promising results for both Imzokitug and Pumitamig individually. Specifically, research indicates that combining Pumitamig with chemotherapy helped up to 70% of patients with advanced NSCLC respond to treatment and kept the disease under control in all evaluable patients. Imzokitug, on the other hand, has improved patient outcomes, particularly by increasing survival rates. These findings suggest that using Imzokitug and Pumitamig, whether separately or together, could effectively treat NSCLC by enhancing patient response to treatment and controlling disease progression.678910
Who Is on the Research Team?
Bristol-Myers Squibb
Principal Investigator
Bristol-Myers Squibb
Are You a Good Fit for This Trial?
This trial is for adults with locally advanced or metastatic non-small cell lung cancer (NSCLC) who have not received prior treatment for their advanced disease. Participants should be healthy enough to receive chemotherapy and meet other medical requirements set by the study.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive Imzokitug in combination with Pumitamig and Platinum-Doublet Chemotherapy (PDCT) or Pumitamig and PDCT alone as first-line treatment for NSCLC
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Imzokitug
- Pumitamig
Trial Overview
The study compares two treatments: one group gets Imzokitug plus Pumitamig and standard platinum-doublet chemotherapy, while the other group receives only Pumitamig with the same chemotherapy. The goal is to see if adding Imzokitug improves outcomes.
How Is the Trial Designed?
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Treatment groups
Experimental Treatment
Find a Clinic Near You
Who Is Running the Clinical Trial?
Bristol-Myers Squibb
Lead Sponsor
Christopher Boerner
Bristol-Myers Squibb
Chief Executive Officer since 2023
PhD in Business Administration from the Haas School of Business, University of California, Berkeley; BA in Economics and History from Washington University in St. Louis
Deepak L. Bhatt
Bristol-Myers Squibb
Chief Medical Officer since 2024
MD from Yale University; MSc in Clinical Epidemiology from the University of Pennsylvania
Citations
Real-World Outcomes and Clinical Predictors of Immune ...
Treatment outcomes included objective response rate, progression-free survival (PFS), and overall survival (OS). with a 5-year survival rate of around 19%.1
Treatment Options for Advanced Non-Small Cell Lung ...
We conducted analyses of the outcomes, costs, and cost-effectiveness of treatment for advanced. NSCLC for two distinct populations: 1. First-line treatment ...
Real-World Outcomes of Patients with Metastatic Non ...
Estimated median overall survival (OS) was 8.0 months (95% confidence interval 7.4-9.0 months). Estimated median OS was 4.7 months
4.
eureka.patsnap.com
eureka.patsnap.com/blog/life-science/small-cell-lung-cancer-competitive-landscape-analysis/Small Cell Lung Cancer — Competitive Landscape
~15–20% of all lung cancers, ~30,000 new US cases annually, and a 5-year overall survival rate below 7% in extensive-stage disease.
'Targeting' Improved Outcomes with Antibody-Drug ...
In this comprehensive review, we will be discussing the recent evidence including targets, efficacy and the safety of newer ADC candidates in NSCLC.
NCT07680764 | A Study To Assess the Safety, Tolerability, ...
A Study To Assess the Safety, Tolerability, and Efficacy of Imzokitug. With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)
7.
trialscreen.org
trialscreen.org/trials/phase-2-to-assess-safety-tolerability-efficacy-imzokitug-combination-pumitamig-trial-nct07680764A Phase 1/2 study of Imzokitug plus Pumitamig and ...
A clinical trial testing whether adding a new medicine (Imzokitug) is safe enough for patients newly diagnosed with advanced or metastatic lung cancer
A Study To Assess the Safety, Tolerability, and Efficacy of ...
This research study is looking at new ways to treat a type of lung cancer called non-small cell lung cancer (NSCLC) that has spread or is advanced.
Efficacy and safety of immune checkpoint inhibitors in non ...
This meta-analysis provides clinical evidence that ICIs improve PFS, OS, and ORR in NSCLC with fewer adverse effects.
Lung Cancer Clinical Trials | BMS Study Connect
Non-small cell lung cancer (NSCLC) accounts for about 85–90% of Lung Cancer diagnoses, Safety, Tolerability, and Efficacy of Imzokitug
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