โšกYour ready-to-use recruitment solution: IRB-compliant, SEO-optimized website that automatically routes qualified patient leads to your clinical study (14-day free trial, then $44/mo)

Limited-duration Teclistamab

Sponsored by Abramson Cancer Center at Penn Medicine

Quick Self-Assessment

See if you qualify and express your interest

Preparing your pre-screening questions...

Current Status

Recruiting

Auto-verified from ClinicalTrials.gov

Verified Oct 1, 2025

Phase

Clinical Trial

Sponsor

Abramson Cancer Center at Penn Medicine

Enrollment Target

75

Start Date

Jul 2023

๐Ÿ“Š
1 of 75 participants interested
1% interest

Express Your Interest Today

Interested in learning more? Complete the form below.

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Advance Medical Science

    Contribute to groundbreaking research

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel (varies by study)

  • Help Others

    Benefit future patients

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3In-person assessment if eligible
  4. 4Begin participation

About This Study

This is a single-arm, non-inferiority study in which patients who have achieved a very good partial response (VGPR) or better, according to International Myeloma Working Group (IMWG) response criteria, following 6 to 9 months of treatment with teclistamab, a B-cell maturation antigen (BCMA)-directed T-cell engager (anti-BCMAxCD3 bispecific antibody), will be offered monitored drug discontinuation.

Who Can Participate

Inclusion Criteria

Participants must be age โ‰ฅ18 and able to give written, informed consent.
Participants must have initiated teclistamab (first full dose) 6-9 months prior to enrollment and received an average teclistamab dose of at least 1.5 mg/kg/month since the date of the first 1.5 mg/kg dose.
Participants must have received a teclistamab dose within 4 weeks prior to enrollment.
Participants must have had measurable disease according to IMWG criteria within 1 month prior to teclistamab initiation or first full teclistamab dose
Participants must have achieved a confirmed VGPR or better to teclistamab therapy at any assessment prior to enrollment and have ongoing response (i.e., no disease progression) at time of enrollment per IMWG consensus criteria (Appendix 14.3).
Prior to initiating teclistamab, participants must have received therapy with a proteasome inhibitor, thalidomide analog (lenalidomide or pomalidomide), and an anti-CD38 antibody and meet one of the follow

โ“ Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility during the screening process.

Study Details

๐Ÿ“‹

Study Type

INTERVENTIONAL

๐Ÿ‘ฅ

Target Enrollment

75 participants

โšง

Gender

ALL

๐Ÿข

Sponsor

Abramson Cancer Center at Penn Medicine

Study Locations

Choose your preferred location or select flexible during enrollment

RECRUITING

Little Rock

Arkansas

Location available
View Little Rock location page
RECRUITING

Iowa City

Iowa

Location available
View Iowa City location page
RECRUITING

New York

New York

Location available
View New York location page
RECRUITING

Philadelphia

Pennsylvania

Location available
View Philadelphia location page
RECRUITING

Philadelphia

Pennsylvania

Location available
View Philadelphia location page

Frequently Asked Questions

Q:What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Q:Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Q:Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Q:Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

Q:How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Still have questions? Our study coordinators are here to help.

Ready to Make a Difference?

Express your interest in this groundbreaking clinical trial

๐Ÿ”’ Secure ยท ๐Ÿฅ Expert Care

Find More Multiple Myeloma Trials by City

Browse all multiple myeloma clinical trials in these cities โ€” not just this study.

Looking for I cannot determine a primary medical condition from this data. The study title mentions "Teclistamab" (a drug) and the listed condition is "OTHER:Off Drug Surveillance" which refers to monitoring rather than a medical condition. There are no keywords or meaningful brief summary provided to identify what health issue this study addresses. Treatment in Iowa City?

Join others in Iowa exploring innovative treatment options through clinical research

I cannot determine a primary medical condition from this data. The study title mentions "Teclistamab" (a drug) and the listed condition is "OTHER:Off Drug Surveillance" which refers to monitoring rather than a medical condition. There are no keywords or meaningful brief summary provided to identify what health issue this study addresses. Treatment Options in Iowa City, Iowa

If you're searching for I cannot determine a primary medical condition from this data. The study title mentions "Teclistamab" (a drug) and the listed condition is "OTHER:Off Drug Surveillance" which refers to monitoring rather than a medical condition. There are no keywords or meaningful brief summary provided to identify what health issue this study addresses. treatment in Iowa City, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Iowa City, New York, Philadelphia and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with I cannot determine a primary medical condition from this data. The study title mentions "Teclistamab" (a drug) and the listed condition is "OTHER:Off Drug Surveillance" which refers to monitoring rather than a medical condition. There are no keywords or meaningful brief summary provided to identify what health issue this study addresses.. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Iowa
Now Enrolling
Up to 75 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for I cannot determine a primary medical condition from this data. The study title mentions "Teclistamab" (a drug) and the listed condition is "OTHER:Off Drug Surveillance" which refers to monitoring rather than a medical condition. There are no keywords or meaningful brief summary provided to identify what health issue this study addresses.?

Potential Benefits

  • โœ“Access to new treatment approaches before public availability
  • โœ“Close monitoring by experienced medical professionals
  • โœ“Study-related care provided at no cost
  • โœ“Contribute to medical research for I cannot determine a primary medical condition from this data. The study title mentions "Teclistamab" (a drug) and the listed condition is "OTHER:Off Drug Surveillance" which refers to monitoring rather than a medical condition. There are no keywords or meaningful brief summary provided to identify what health issue this study addresses.

What to Expect

  • โ†’Initial screening to determine eligibility
  • โ†’Regular check-ups and monitoring visits
  • โ†’Possible compensation for time and travel
  • โ†’You can withdraw at any time

Frequently Asked Questions About This I cannot determine a primary medical condition from this data. The study title mentions "Teclistamab" (a drug) and the listed condition is "OTHER:Off Drug Surveillance" which refers to monitoring rather than a medical condition. There are no keywords or meaningful brief summary provided to identify what health issue this study addresses. Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT05932680. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.