Autopsy report · NCT05042934

Lurbinectedin With or Without Irinotecan in Treating Patients With Relapsed or High Risk Metastatic Ewing Sarcoma

“PI stated trial no longer fits the framework \& portfolio of work that is prioritized by the department. PI will not have the anticipated accrual in PI view to complete the study. Given that, PI request this protocol be closed prior to its activation.”

The sponsor’s own words in the registry.

Life of this trial

• Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.

Vital statistics

Status

Withdrawn

Phase

Phase 1, Phase 2

Sponsor

M.D. Anderson Cancer Center

Sponsor type

University, hospital or other

Conditions

Metastatic Ewing Sarcoma; Recurrent Ewing Sarcoma

Interventions

Fine-Needle Aspiration; Irinotecan; Irinotecan Hydrochloride; Lurbinectedin

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Fludeoxyglucose F 18 PET/CT Scans in Predicting Therapy Response in Patients With Stage IIIA Non-Small Cell Lung Cancer Undergoing Chemoradiation
  “No subjects have been accrued to this trial. The PI will no longer be at COH and requests a study withdrawal/closure.” (75% match in meaning)
• Surface EMG Biofeedback for Children With Cerebral Palsy
  “The PI for this trial, which has been terminated, is no longer employed by USC. After repeated attempts of contact, we are unable to identify the PI's current employment. We would therefore request close out of this clinical trial record.” (69% match in meaning)
• HIV-1 Vaccine Test in Uninfected Adult Volunteers
  “The study product was revised. PI withdrew the study without enrolling participants..” (66% match in meaning)
• Investigational TMS Treatment for Depression
  “PI's discretion due to needing to modify study protocol.” (66% match in meaning)
• Maternal Epidural Steroids and Hyperthemia
  “PI permanently closed accrual for the study based on FDA warning issued in April 2014. Study is closed” (66% match in meaning)

Look deeper

• The official registry record (the source of truth)
• Record history: every change the sponsor made
• Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.