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Recruiting Phase 4 NCT07133074

NCT07133074 Allergy Delabeling in Antibiotic Stewardship - Intervention

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Clinical Trial Summary
NCT ID NCT07133074
Status Recruiting
Phase Phase 4
Sponsor Abramson Cancer Center at Penn Medicine
Condition Beta Lactam Allergy
Study Type INTERVENTIONAL
Enrollment 3,800 participants
Start Date 2026-04-20
Primary Completion 2028-11

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
RENEW-IN Algorithm for assessment of a beta-lactam interventionEMR Review

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 4 studies follow an already-approved treatment in real-world conditions to monitor long-term safety and effectiveness.

This trial targets 3,800 participants in total. It began in 2026-04-20 with a primary completion date of 2028-11.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The overall goal of the RENEW-IN intervention is to assess the impact of a BL allergy delabeling intervention on antibiotic use and clinical outcomes in patients with a hematologic malignancy.

Eligibility Criteria

Inclusion Criteria: * all patients with a hematologic malignancy (including Hodgkin and non-Hodgkin lymphoma, leukemia, and myeloma) admitted to an inpatient oncology service * reported history of a beta-lactam (BL) allergy (i.e., penicillin, cephalosporin, and/or carbapenem) Exclusion Criteria: * patients with a history of severe cutaneous adverse reaction * patients with a history of Stevens-Johnson syndrome * patients with a history of toxic epidermal necrolysis * patients with a history of drug-induced exfoliative dermatitis * patients with a history of drug reaction with eosinophilia and systemic symptoms * patients with a history of acute generalized exanthematous pustulosis

Contact & Investigator

Central Contact

Ebbing Lautenbach, MD,MPH,MSCE

✉ ebbing@pennmedicine.upenn.edu

📞 215-898-6977

Frequently Asked Questions

Who can join the NCT07133074 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Beta Lactam Allergy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07133074 trial and what does that mean for participants?

Phase 4 studies are conducted after a treatment has been approved. They monitor long-term safety and real-world effectiveness in a broader patient population.

Is NCT07133074 currently recruiting?

Yes, NCT07133074 is actively recruiting participants. Contact the research team at ebbing@pennmedicine.upenn.edu for enrollment information.

Where is the NCT07133074 trial being conducted?

This trial is being conducted at Philadelphia, United States.

Who is sponsoring the NCT07133074 clinical trial?

NCT07133074 is sponsored by Abramson Cancer Center at Penn Medicine. The trial plans to enroll 3,800 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology