A Study of Pasireotide in People With Prolactinoma

PHASE2RecruitingINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

February 27, 2024

Primary Completion Date

February 28, 2027

Study Completion Date

February 28, 2027

Conditions
Prolactin-Producing Pituitary Tumor
Interventions
DRUG

Pasireotide

Pasireotide will be initiated at 40 mg IM one time dose and if tolerated dose will be increased to 60 mg IM every 4 weeks +/-7 days.

OTHER

SF-36 and HADS

Baseline assessment will be conducted within 30 days of starting treatment, week 12, 24 and week 28.

Trial Locations (7)

10065

RECRUITING

Memorial Sloan Kettering Cancer Center, New York

10604

RECRUITING

Memorial Sloan Kettering Westchester (Limited Protocol Activities), Harrison

11553

RECRUITING

Memorial Sloan Kettering Nassau (Limited Protocol Activities), Uniondale

11725

RECRUITING

Memorial Sloan Kettering Suffolk-Commack (Limited Protocol Activities), Commack

07920

RECRUITING

Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities), Basking Ridge

07748

RECRUITING

Memorial Sloan Kettering Monmouth (Limited Protocol Activities), Middletown

07645

RECRUITING

Memorial Sloan Kettering Bergen (Limited Protocol Activities), Montvale

All Listed Sponsors
collaborator

RECORDATI GROUP

INDUSTRY

lead

Memorial Sloan Kettering Cancer Center

OTHER