About this trial

A Phase 2 multi-center, open-label, single arm study of nab-sirolimus in patients with well-differentiated neuroendocrine tumors (NETs) of the gastrointestinal tract, lung, or pancreas who have not received prior treatment with mTOR inhibitors

Eligibility criteria

Qualifiers

Patients with functional or non-functional, well-differentiated, locally advanced unresectable or metastatic NETs of the GI tract, lung, or pancreas who have received 2 or less prior lines of therapy excluding somatostatin analogs

the patient has been on a stable dose of an somatostatin analogs for ≥12 weeks and

the patient has experienced disease progression while on stable somatostatin analogs dose

Patients must have 1 or more measurable target lesions by RECIST v1.1

Disqualifiers

Prior treatment with mTOR inhibitors including nab-sirolimus

Patients with functional NETs who are experiencing uncontrolled symptoms attributed to hormones and other vasoactive substances secreted by the tumor

Patients with inactivating TSC1 or TSC2 alterations (based on tissue or liquid NGS)

Severe (Grade ≥3) ongoing infection requiring parenteral or oral anti-infective treatment, either ongoing or completed ≤7 days prior to enrollment

Trial design

Treatments tested in this trial

  • nab-sirolimus

Treatment groups

21 Participants
are divided into 1 treatment group

Locations

4
Hoag Memorial Hospital Presbyterian92663, Newport BeachCalifornia, United States
Rocky Mountain Cancer Centers80218, DenverColorado, United States
Texas Oncology75246, DallasTexas, United States
Medical College of Wisconsin Cancer Center53226, MilwaukeeWisconsin, United States

Sponsors and collaborators

Aadi Bioscience, Inc.

Lead sponsor