Information for current Syncromune clinical trial participants, past clinical trial participants, caregivers, and family members.
Clinical trial volunteers make the development of new cancer therapies possible. We appreciate your strength and commitment because, without people like you, life-changing breakthroughs could not happen. Syncromune provides information to help you make an informed choice about participating in research trials. Be sure to discuss these topics with your healthcare provider.
Every clinical trial is different and so the way you prepare and participate depends on your specific trial. Below is some supplemental information and resources to consider as you navigate this process.
Clinical trial volunteers make the development of new cancer therapies possible. We appreciate your strength and commitment because, without people like you, life-changing breakthroughs could not happen. Syncromune provides information to help you make an informed choice about participating in research trials. Be sure to discuss these topics with your healthcare provider.
Every clinical trial is different and so the way you prepare and participate depends on your specific trial. Below is some supplemental information and resources to consider as you navigate this process.
As part of your enrollment in a Syncromune clinical trial, you have an entire team to support your participation including the site location, investigators, and primary points of contact who will help you navigate your treatment.
Clinical trial participants play a crucial role in developing new cancer therapies and we are committed to upholding the highest ethical standards to protect the safety, privacy, and confidentiality of you and your loved ones.
The clinical teams that conduct trials follow the same rules and regulations as other healthcare providers as well as federal government requirements and regulations. In every trial plan and protocol there are protections built into the trial processes that function to safeguard the wellbeing of participants. You have several rights as a participant, including but not limited to:
Confidentiality and protected identity
Ability to leave the trial at any time
Know all possible risks and benefits
Ask questions about all aspects of the trial
Confidentiality and protected identity
Ability to leave the trial at any time
Know all possible risks and benefits
Ask questions about all aspects of the trial
The trial coordinator or another member of the trial team at the site location where you are participating is typically your main point of contact throughout the clinical trial. This member can answer many questions general questions about your trial such as the date of your next treatment or follow-up imaging. Depending on your question, you may be referred to other members of the study team, such as the principal investigator at your trial site.
You should seek medical assistance immediately and inform the healthcare professionals that provide care that you are in a clinical trial. You can provide the contact information for your Syncromune clinical trial team so the healthcare professionals can speak with someone about the therapy you are receiving.
The available support can vary based on which trial you are participating in and the location of the trial site. This may include items like access to digital tools, transportation, and resources to assist in your trial participation. In addition, ready access to the trial team is available to answer any questions you may have.
The SYNC-T Therapy is an entirely new approach to treating metastatic solid tumor cancers. It is an in situ (within the body) personalized therapy that combines freezing of a portion of a tumor followed by the infusion of a drug directly into the tumor. The goal is to activate the immune system and combat cancer in several different ways. This combination approach is designed to empower your immune system to recognize and attack cancer throughout the body.Â
You should contact your clinical trial site team as soon as the side effect happens and follow any instructions provided. The team may determine that you need additional procedures or medications. All side effects should be reported to the clinical trial team, even if the symptoms are mild or you think that were not caused by the trial therapy.Â
Yes, taking part in any clinical trial is completely voluntary. If you decide to take part, you are free to withdraw at any time, for any reason, and without any penalty or effect on your future medical care. If you decide to leave your trial, you should talk to your physician about next steps.
The information you provide, imaging, and other medically-related exams will not be shared with anyone who is not directly associated with the LEGION-100 trial without your permission, except as set forth in the informed consent which will be reviewed with you in detail by the clinical trial team.
If you have general questions about your trial, you can contact the Syncromune clinical team via this contact form. For specific questions, please contact your assigned trial site team member.
Clinical trial volunteers make the development of new cancer therapies possible. We appreciate your dedication and time commitment to help develop life-changing breakthroughs and contribute to change patient’s lives around the world.
Depending on the trial design, once you have completed your participation in the clinical trial you will need to wait for other participants to complete their treatment before the results of the trial can be determined.
Clinical trial volunteers make the development of new cancer therapies possible. We appreciate your dedication and time commitment to help develop life-changing breakthroughs and contribute to change patient’s lives around the world.
Depending on the trial design, once you have completed your participation in the clinical trial you will need to wait for other participants to complete their treatment before the results of the trial can be determined.
The results of your trial may help to determine the next steps of the therapy, such as advancing to the next phase of clinical trials to continue researching the therapy. If the safety and efficacy data from trials of the new investigational therapy meets certain criteria, an application will be submitted to the FDA and other regulatory authorities for potential approval to use in patients. Therapies often take several years to complete this process.
As a caregiver of a participant in a clinical trial, you play an important role in supporting your friend or family member. The comfort and care that you provide can help improve your loved one’s successful completion of their clinical trial and potentially have a positive impact on their health. We hope the provided information is helpful as you prepare to assist your family member or friend.
As a caregiver of a participant in a clinical trial, you play an important role in supporting your friend or family member. The comfort and care that you provide can help improve your loved one’s successful completion of their clinical trial and potentially have a positive impact on their health. We hope the provided information is helpful as you prepare to assist your family member or friend.
There are numerous prostate cancer advocacy groups and other cancer resources that provide extensive information about the disease, cancer in general, current treatment options based on cancer stage, and support groups designed to help patients and caregivers. For your reference, below is a list of of some organizations along with links to their websites
There are numerous prostate cancer advocacy groups and other cancer resources that provide extensive information about the disease, cancer in general, current treatment options based on cancer stage, and support groups designed to help patients and caregivers. For your reference, below is a list of of some organizations along with links to their websites
For Prostate Cancer
For Prostate Cancer
For Prostate Cancer
Syncromune Clinical Team Contact Form
This form is intended for current and past clinical trial participants who have general questions. If you have a specific question about your trial, please contact your assigned trial site team member.