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NCT05660616CompletedPhase 2

Switch-Maintenance Gemcitabine After First-Line Chemotherapy In Patients With Malignant Pleural Mesothelioma

Switch-Maintenance Gemcitabine After First-Line Chemotherapy (Pemetrexed-Platinum) In Patients With Malignant Pleural Mesothelioma In Ain Shams University Hospitals

Source: ClinicalTrials.gov · Last updated 27 Aug 2024

Brief summary (registry, in English)

Mesothelioma is an aggressive form of cancer. Treatments are available, but for many people, a cure isn't possible. This thesis is to assess the efficacy and safety of switch-maintenance Gemcitabine in Mesothelioma patients after first line chemotherapy (Pemetrexed-Platinum)

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
40 (actual)
First submitted
5 Dec 2022
Start date
1 Apr 2023
Primary completion date
1 Apr 2024
Lead sponsor
Ain Shams University
NCT number
NCT05660616

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 40
  • From 1 Apr 2023 to the primary completion date, 1 Apr 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who are candidates for curative surgery

Other illness

  • Progression of disease after first line

Other

  • Pregnant females
  • ECOG Performance 3-4
  • Patients with sarcomatoid mesothelioma

Who the study is looking for

  • Being at least 18 years old
  • Histologically or cytologically confirmed unresectable malignant pleural mesothelioma
  • ECOG Performance status 0-2
  • Completed at least four cycles of first line platinum (cisplatin or carboplatin) and pemetrexed combination chemotherapy before study entry
  • No evidence of disease progression following first-line treatment based on radiological criteria.
  • Adequate organ function is mandatory, defined as haemoglobin of at least 8.5 mg/dl, platelets of at least 100×10⁹ per L, and neutrophils of at least 1×10⁹/L.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ain Shams University Hospital
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.