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NCT05477576Active, not recruitingPhase 3

Study of RYZ101 Compared With SOC in Pts w Inoperable SSTR+ Well-differentiated GEP-NET That Has Progressed Following 177Lu-SSA Therapy

Phase 1b/3 Global, Randomized, Controlled, Open-label Trial Comparing Treatment With RYZ101 to Standard of Care Therapy in Subjects With Inoperable, Advanced, SSTR+, Well-differentiated GEP-NETs That Have Progressed Following Prior 177Lu-SSA Therapy

Source: ClinicalTrials.gov · Last updated 5 Oct 2026

Brief summary (registry, in English)

This study aims to determine the safety, pharmacokinetics (PK) and recommended Phase 3 dose (RP3D) of RYZ101 in Part 1, and the safety, efficacy, and PK of RYZ101 compared with investigator-selected standard of care (SoC) therapy in Part 2 in subjects with inoperable, advanced, well-differentiated, somatostatin receptor expressing (SSTR+) gastroenteropancreatic neuroendocrine tumors (GEP-NETs) that have progressed following treatment with Lutetium 177-labelled somatostatin analogue (177Lu-SSA) therapy, such as 177Lu-DOTATATE or 177Lu-DOTATOC (177Lu-DOTATATE/TOC), or 177Lu-high affinity \[HA\]-DOTATATE.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
343 (actual)
First submitted
20 Jul 2022
Start date
24 Mar 2022
Primary completion date
Dec 2026
Lead sponsor
RayzeBio, Inc.
NCT number
NCT05477576

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 343
  • From 24 Mar 2022 to the primary completion date, Dec 2026
  • 52 sites in 8 countries
  • 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.

Criteria the registry did not label

  • Inclusion:
  • Histologically proven, Grade 1-2 well differentiated, inoperable, advanced GEP-NETs (Ki67 ≤20%) Eastern Cooperative Oncology Group (ECOG) status 0-2. Ki67% \<20% is not required for the ad hoc subcohort of the PK/ECG substudy.
  • Progressive, SSTR-PET positive (i.e., Krenning score 3 or 4) GEP-NET (GI or pancreas) following 2-4 cycles of treatment with 177Lu-labeled SSA. Must have achieved disease control for at least 6 months following Lu-177 SSA (archival tissue is not required for the ad hoc subcohort of the PK/ECG substudy). No time limit is defined between 177Lu-SSA treatment and randomization. There must be at least 1 SSTR-PET imaging-positive measurable site of disease (according to RECIST v1.1) and no RECIST v1.1 measurable metastatic lesions that are SSTR imaging-negative.
  • Adequate renal function, as evidenced by estimated glomerular filtration rate (eGFR) ≥60 mL/min/1.73 m2 (calculated using the Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\]) (Levey et al. 2009)
  • Adequate hematologic function, defined by the following laboratory results:
  • Part 2: Hemoglobin concentration ≥5.0 mmol/L (≥8.0 g/dL); ANC ≥1000 cells/µL (≥1000 cells/mm3); platelets ≥75 x 109/L (75 x 103/mm3).
  • Total bilirubin ≤3 x upper limit normal (ULN)
  • Serum albumin ≥3.0 g/dL unless prothrombin time is within the normal range
    • Exclusion:
  • Prior radioembolization
  • Significant cardiovascular disease, such as New York Heart Association (NYHA) Class ≥II heart failure, left ventricular ejection fraction (LVEF) \<40% or QT interval corrected for heart rate using Fridericia's formula (QTcF) \>450 ms for males and \>470 ms for females.
  • Resistant hypertension, defined as uncontrolled blood pressure (BP) \>140/90 mmHg while on optimal doses of at least 3 antihypertensive medications with 1 being a diuretic (Whelton et al. 2018)
  • Uncontrolled diabetes mellitus as defined by hemoglobin A1C (HgB A1C) ≥8%
  • PRRT other than Lu-177 SSA (not applicable for ad hoc subcohort of the PK/ECG substudy)
  • Any condition requiring systemic treatment with high-dose glucocorticoids within 14 days prior to first dose of study treatment and/or which cannot be stopped while on study. Inhaled or topical steroids are permitted.
  • Prior history of liver cirrhosis or liver transplantation

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

Full criteria on ClinicalTrials.gov

Sites (52)

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

SiteCityCountrySite status
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BrusselsBelgiumUnknown status
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LeuvenBelgiumUnknown status
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RoeselareBelgiumUnknown status
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BrasíliaBrazilUnknown status
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Rio de JaneiroBrazilUnknown status
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São PauloBrazilUnknown status
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LondonCanadaUnknown status
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MontrealCanadaUnknown status
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TorontoCanadaUnknown status
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BarcelonaSpainUnknown status
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MadridSpainUnknown status
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ZaragozaSpainUnknown status
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ClichyFranceUnknown status
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LilleFranceUnknown status
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MontpellierFranceUnknown status
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NantesFranceUnknown status
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Vandœuvre-lès-NancyFranceUnknown status
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VillejuifFranceUnknown status
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SeoulSouth KoreaUnknown status
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AmsterdamNetherlandsUnknown status
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MaastrichtNetherlandsUnknown status
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UtrechtNetherlandsUnknown status
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AtlantaUnited StatesUnknown status
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BostonUnited StatesUnknown status
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ClevelandUnited StatesUnknown status
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ColumbusUnited StatesUnknown status
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DuarteUnited StatesUnknown status
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Glen BurnieUnited StatesUnknown status
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HoustonUnited StatesUnknown status
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Iowa CityUnited StatesUnknown status
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IrvineUnited StatesUnknown status
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JacksonvilleUnited StatesUnknown status
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LexingtonUnited StatesUnknown status
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Los AngelesUnited StatesUnknown status
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MiamiUnited StatesUnknown status
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NashvilleUnited StatesUnknown status
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New HavenUnited StatesUnknown status
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New YorkUnited StatesUnknown status
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OmahaUnited StatesUnknown status
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Palo AltoUnited StatesUnknown status
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PhiladelphiaUnited StatesUnknown status
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PhoenixUnited StatesUnknown status
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PittsburghUnited StatesUnknown status
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PortlandUnited StatesUnknown status
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RochesterUnited StatesUnknown status
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Salt Lake CityUnited StatesUnknown status
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San FranciscoUnited StatesUnknown status
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SeattleUnited StatesUnknown status
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St LouisUnited StatesUnknown status
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TampaUnited StatesUnknown status
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TroyUnited StatesUnknown status
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Washington D.C.United StatesUnknown status

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