Partner with Effectus to support a nearby clinical trial for patients with advanced or metastatic solid tumor malignancies or lymphoma.
Provide your contact information below and a member of the Effectus team will reach out with program details. Should you have any questions prior, please call us directly at 973-753-2430.
About the Clinical Trial
Moderna’s Phase 1 dose escalation research trial is evaluating the safety and tolerability of mRNA-2752 administered alone and in combination with durvalumab for patients with advanced or metastatic solid tumor malignancies or lymphoma.
How You Can Get Involved
As a health care provider (HCP) who sees adult patients with advanced or metastatic solid tumor malignancies or lymphoma, you are invited to participate in the Effectus Patient Identification and Consultation Program to help identify candidates for the Moderna mRNA-2752-P101 trial. You will be asked to consult with patients in a neutral manner about the trial and assess their interest in participating at a nearby trial site. Patients may be able to take part if they are 18 years of age or older and meet additional high-level criteria (key trial criteria will be provided to you upon onboarding). At the trial site, patients will undergo trial screening to determine eligibility.
Compensation at fair market value will be available for HCPs who participate and meet program requirements.
Support Provided
Effectus will be your trusted partner throughout your participation, helping to facilitate your patients to the trial site and thus relieving the burden on your practice. If you wish to participate, you will be asked to review and sign a Services Agreement with Effectus, which outlines your program responsibilities and compensation. Participation is completely voluntary, and you can opt out at any time. Background on the trial, program materials, and program logistics will be reviewed in detail during a 1-hour virtual training session.
Why You Should Participate
The Moderna mRNA-2752-P101 trial provides an opportunity to contribute to the research and advancement of a potential new treatment option for patients with advanced or metastatic solid tumor malignancies or lymphoma. The trial also allows HCPs the opportunity to offer alternative treatment options to their patients.
The Effectus Patient Identification and Consultation Program
Effectus Patient Identification and Consultation Program Overview
Sign a services
agreement.
Receive a package of
program materials and
complete a simple, one-hour
virtual training session.
Utilize key screening
criteria to identify
potentially eligible
patients.
If the patient meets the criteria,
conduct a neutral consultation
about the availability of the
nearby trial and gauge the
patient’s interest.
If the patient is interested in
participation, our team of dedicated
Patient Facilitators help ensure a
smooth patient transfer from your
office to the clinical trial site.
The patient is scheduled
and presents at the trial
site for the screening
appointment.
The patient’s enrollment
status is determined and is
relayed back to the treating
HCP by Effectus.
For more information on our program, please visit https://www.effectusctr.com/physician-network/.
Contact Us
Montana Markell, Project Coordinator
Phone: 973-753-2430
Email: mmarkell@effectusctr.com
How can you get involved? It’s easy!
Want to learn about available programs near you? Contact Effectus today to become part of our growing network of health care providers, allowing you to participate in programs and learn about the latest developments in clinical research.
…or contact us for more information.
Effectus Clinical Trial Recruitment
89 Headquarters Plaza
Suite #1450
Morristown, NJ 07960