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Clinical trialNCT06456359RecruitingPhase 2Interventional

Pasireotide as Maintenance Treatment in Synovial Sarcoma and Desmoplastic Small Round Cell Tumor

SponsorUniversity Hospital HeidelbergEnrollment28Desmoplastic Small Round Cell TumorSynovial Sarcoma
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

PAMSARC is a non-commercial interventional Phase 2 clinical trial of academic research institutions, with its primary goal being to improve medical treatment of fusion driven Desmoplastic small round cell tumor (DSRCT) and Synovial sarcoma (SySa) in young adults and adolsecents with male predominance. Current management of DSRCT and SySa includes chemotherapy, radiation and aggressive cytoreductive surgery. Despite advances in multimodal therapy, outcomes remain poor with frequent disease recurrence and very limited options for patients with advanced disease. Selected somatostatin receptor (SSTR) family members, i.e., SSTR2, SSTR3 and SSTR5, are frequently overexpressed in DSRCT and SySa, providing the rationale for treatment with somatostatin analogues (SSA). Pasireotide is a SSA with high affinity for SSTR1, -2, -3, and -5 and is approved for the treatment of Cushing's disease and acromegaly and has also shown activity in other cancers. In patients with advanced stage DSRCT and SySa, conventional chemotherapeutic approaches frequently lead to disease response, however, the duration of progression-free time after chemotherapy is short. The targeted approach with pasireotide after initial intensive multimodal treatment may have the potential to significantly improve outcome.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Richard F. Schlenk, Professor

    National Center for Tumour Diseases, University Hospital Heidelberg

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Germany
  • National Center for Tumour Diseases, University Hospital Heidelberg

    Heidelberg, Baden-Wurttemberg, Germany

    Richard F. Schlenk, Prof. Dr. med.
    Recruiting
  • Klinikum Stuttgart Studienzentrale Stuttgart Cancer Center, Tumorzentrum Eva-Mayr-Stihl

    Stuttgart, Baden-Wurttemberg, Germany

    Dennis Hahn, M.D.
    Not, yet, recruiting
  • Klinikum Stuttgart- Olga Hospital Zentrum Für Kinder-, Jugend Und Frauenmedizin

    Stuttgart, Baden-Wurttemberg, Germany

    Monika Sparber-Sauer, Prof. Dr. med.
    Not, yet, recruiting
  • Universitätsklinikum Essen Pädiatrische Hämatologie Und Onkologie

    Essen, North Rhine-Westphalia, Germany

    Uta Dirksen, Prof. Dr. med
    Not, yet, recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Signifor
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
19 Dec 2024
Primary completion
31 Oct 2027
Completion
31 Oct 2028
Last update posted
13 Jan 2025
Registered enrollment
28
Registry id
NCT06456359

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.