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Mistletoe Extract for Advanced Lung Cancer
Phase 2
Waitlist Available
Research Sponsored by Sidney Kimmel Cancer Center at Thomas Jefferson University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients with Stage IIIB or IV non-small cell lung cancer
Planning to receive standard chemotherapy with either carboplatin plus paclitaxel or cisplatin plus gemcitabine
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial is testing if mistletoe extract can help build an immune response and improve quality of life for patients with stage IIIB or IV non-small cell lung cancer receiving palliative chemotherapy.
Who is the study for?
This trial is for adults over 18 with advanced non-small cell lung cancer (stage IIIB or IV) who are starting palliative chemotherapy. They must be able to self-report their quality of life and have a Karnofsky performance status between 60-100%. Patients already on immunosuppressives, steroids, mistletoe products, or other clinical trials cannot join.Check my eligibility
What is being tested?
The study is testing the effectiveness of mistletoe in improving immune response and quality of life in patients undergoing standard palliative chemotherapy for advanced non-small cell lung cancer. It's a phase II trial to see how well it works alongside chemo drugs like carboplatin plus paclitaxel or cisplatin plus gemcitabine.See study design
What are the potential side effects?
While specific side effects of mistletoe are not detailed here, common ones may include injection site reactions, headaches, feverish symptoms. As this is an adjunct therapy to chemotherapy, typical chemo-related side effects such as nausea, fatigue and increased infection risk may also occur.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My lung cancer is at stage IIIB or IV.
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I am planning to undergo chemotherapy with carboplatin and paclitaxel or cisplatin and gemcitabine.
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My condition was recently diagnosed.
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I am not participating in any experimental chemotherapy trials.
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I can care for myself but may not be able to do active work.
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I am 18 years old or older.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Find a Location
Who is running the clinical trial?
National Cancer Institute (NCI)NIH
13,667 Previous Clinical Trials
40,926,166 Total Patients Enrolled
Sidney Kimmel Cancer Center at Thomas Jefferson UniversityLead Sponsor
162 Previous Clinical Trials
10,911 Total Patients Enrolled
Steven Rosenzweig, MDStudy ChairSidney Kimmel Cancer Center at Thomas Jefferson University
1 Previous Clinical Trials
36 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My lung cancer is at stage IIIB or IV.I am planning to undergo chemotherapy with carboplatin and paclitaxel or cisplatin and gemcitabine.I can care for myself but may not be able to do active work.I haven't had cancer in the last 5 years, except for skin cancer.I have had a condition where my lymphocytes grow abnormally.My condition was recently diagnosed.I am not participating in any experimental chemotherapy trials.I can describe my own quality of life.I am 18 years old or older.I have a history of cancer.
Research Study Groups:
This trial has the following groups: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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What assurances can you provide regarding the safety of this treatment?
"The safety profile of this treatment is ranked at 2, as the Phase 2 trial only has limited data proving its security and no evidence to attest for efficacy."
Answered by AI
Is this scientific experiment ongoing and open to participants?
"Per clinicaltrials.gov, this medical trial is no longer enrolling; originally posted on October 1st 2002 and updated as recently as December 17th 2013. Despite being closed to recruitment, there are still 1626 other studies actively seeking candidates at the moment."
Answered by AI
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