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NCT05813132
BeEAM Versus CEM in Lymphoma Patients as a Conditioning Regimen Before Autologous Hematopoietic Cell Transplantation
NA trial testing BEAM Protocol in Lymphoma in 58 participants. Completed in 30 December 2023.
30 December 2023
Quick facts
| Lead sponsor | Rehab Werida |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 58 |
| Start date | 11 November 2022 |
| Primary completion | 30 December 2023 |
| Estimated completion | 30 December 2023 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- BEAM Protocol — full drug profile →
- CEM protocol — full drug profile →
Conditions studied
- Lymphoma — all drugs for Lymphoma →
Sponsor
Rehab Werida — full company profile →
Who can join
Adults 18 to 70, any sex, with Lymphoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The proposed research aims to compare between BeEAM standard regimen and CEM as conditioning regimen in lymphoma patients in safety profile\& toxicity, infections (Febrile neutropenia) during transplant, time to engraftment (recovery not neutropenic), Length of stay at hospital, time to relapse, and other complications.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Clinical and safety outcomes of BeEAM (Bendamustine, Etoposide, Cytarabine, Melphalan) versus CEM (Carboplatin, Etoposide, Melphalan) in lymphoma patients as a conditioning regimen before autologous hematopoietic cell transplantation.
Eltelbanei MA, El-Bassiouny NA, Abdalla MS, Khalaf M, et al · · 2024 · cited 1× · PMID 39134959 · DOI 10.1186/s12885-024-12694-9
Verify or expand the search:
- PubMed search for NCT05813132
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Rehab Werida trials
Trials by the same sponsor.
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- NCT05459389 — Early Targeted Antibiotic Therapy in Patients With Sepsis · NA · completed
- NCT05291039 — Infliximab and Adalimumab in Inflammatory Bowel Disease Patients. · NA · completed
- NCT05291338 — Pharmacogenetic Study in Hepatocellular Carcinoma Patients. · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05813132 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Rehab Werida
- Last refreshed: 5 September 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05813132.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing