Study of ORIC-533 in Relapsed or Refractory Multiple Myeloma

Relapsed or Refractory Multiple Myeloma Clinical Trial

Official title:

An Open-label Phase 1b Study of ORIC-533 in Patients With Relapsed or Refractory Multiple Myeloma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05227144
• Other study ID #: ORIC-533-01
• Status: Recruiting
• Phase: Phase 1
• Start date: January 6, 2022
• Est. completion date: June 2024

Study information

• Verified date: September 2023
• Source: ORIC Pharmaceuticals
• Contact: ORIC Clinical
• Phone: 650-388-5600
• Email: clinical[@]oricpharma.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to establish the Recommended Phase 2 Dose (RP2D), safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antimyeloma activity of ORIC-533 in patients with multiple myeloma who have exhausted available treatment options

Description:

ORIC-533 is a selective, orally bioavailable, small molecule inhibitor of CD73.This is an open-label, uncontrolled, multicenter, dose-finding study to assess the safety and preliminary antimyeloma activity of ORIC-533 in patients with relapsed or refractory multiple myeloma. After the RP2D has been determined, dose expansion will further evaluate safety and preliminary antimyeloma activity of ORIC-533 in patients with relapsed or refractory multiple myeloma.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 56
• Est. completion date: June 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of multiple myeloma (MM) with relapsed or refractory disease according to IMWG Criteria
• Refractory to or not eligible for MM treatment regimens known to provide clinical benefit, including but not limited to an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 antibody, with documented disease progression
• Measurable disease at screening, including at least 1 of the criteria below:
• Serum M-protein >0.5 g/dL (Patients with IgA myeloma in whom serum M protein is unreliable due to comigration of normal serum proteins may be considered eligible if total IgA >400 mg/dL)
• Urine M-protein >200 mg/24 hours
• Serum free light chains (FLC) assay: Involved FLC assay =10 mg/dL (=100 mg/L) and an abnormal serum FLC ratio (<0.26 or >1.65)
• Measurable bone or extramedullary plasmacytoma
• ECOG performance status =2
• Adequate bone marrow, renal, hepatic, pulmonary, and cardiac function defined as:
• Estimated glomerular filtration rate =40 mL/min/1.73 m2.
• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels both =3 times of upper limit of normal, unless there is suspected disease in the liver, in which case, no limit is set provided serum bilirubin is within eligibility criterion
• Total bilirubin <1.5 × upper limit of normal (ULN), except in study participants with Gilbert's syndrome
• Platelet count >40,000/µL
• Absolute neutrophil count (ANC) >1000/µL
• Left ventricular ejection fraction (LVEF) >45% as assessed by echocardiogram (ECHO) or multiple gated acquisition (MUGA)
• Baseline oxygen saturation >92% on room air

Exclusion Criteria:

• Diagnosed or treated for another malignancy within 3 years prior to enrollment, with the exception of complete resection of basal cell carcinoma or squamous cell carcinoma of the skin, an in situ malignancy, or low risk prostate cancer after curative therapy
• Previous or concurrent plasma cell leukemia, AL amyloidosis, or POEMS (polyneuropathy, organomegaly, endocrinopathy, and skin changes) syndrome
• Known central nervous system (CNS) involvement
• Evidence of hyperviscosity syndrome
• Receiving any investigational treatment with a novel investigational agent (ie, no approved indication) within 28 days prior to the first dose of study drug
• Not recovered or stabilized from all toxicities from prior anticancer therapies and/or radiotherapy to Grade <2 with the exception of peripheral neuropathy
• Major surgery or radiation therapy within 14 days prior to first dose of study drug or incomplete recovery from adverse effects resulting from such procedure
• Those who require limited course of radiation for management of bone pain for =14 days from initiation of therapy are not excluded
• Infection requiring systemic antibiotic therapy or other serious infection within 14 days of starting therapy
• Those who are on prophylactic antibiotics only, or on antibiotics and have confirmation of resolution of active infection, are eligible
• Daily requirement for corticosteroids (equivalent to >10 mg/day prednisone). Inhalation corticosteroids are exempt from this criterion
• Exception: Corticosteroid dose equivalent >10 mg/day prednisone is acceptable if physiological levels require, so long as the dose is stable for at least 7 days prior to initiation of therapy
• Lower amounts of corticosteroids that are not part of a daily requirement within 14 days prior to initiating therapy are also acceptable
• Known seropositive for active viral infection with human immunodeficiency virus (HIV), hepatitis B (HBV), or hepatitis C virus (HCV). Those who are seropositive because of hepatitis B vaccine are eligible. Patients who are positive for HBV core antibody or HBV surface antigen must have a negative polymerase chain reaction (PCR) result prior to enrollment. Those who are PCR positive will be excluded.
• History of class III or IV congestive heart failure or severe non-ischemic cardiomyopathy, unstable or poorly controlled angina, myocardial infarction, or ventricular arrhythmia within the previous 6 months of first dose of study drug
• QTcF >470 msec
• Other concurrent serious uncontrolled medical, psychological, or addictive conditions that, in the opinion of the investigator, may interfere with protocol compliance or contraindicates participation in the study

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell
• Relapsed or Refractory Multiple Myeloma

Intervention

Drug:
• ORIC-533
ORIC-533 once daily in consecutive 28-day cycles

Locations

Country	Name	City	State
Canada	Princess Margaret Cancer Research Center/University Health Network	Toronto	Ontario
United States	Northside Hospital Cancer Institute	Atlanta	Georgia
United States	Dana-Farber Cancer Institute	Boston	Massachusetts
United States	The Charlotte-Mecklenburg Hospital Authority d/b/a Atrium Health	Charlotte	North Carolina
United States	Icahn School of Medicine at Mount Sinai	New York	New York
United States	Mayo Clinical Rochester	Rochester	Minnesota
United States	Swedish Health Services	Seattle	Washington
United States	James R. Berenson, MD, Inc.	West Hollywood	California

Sponsors (1)

Lead Sponsor	Collaborator
ORIC Pharmaceuticals

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Recommended Phase 2 Dose (RP2D)	RP2D as determined by interval 3+3 dose escalation design	12 months
Primary	Number of participants with adverse events	Safety and tolerability of ORIC-533	36 months
Primary	Number of participants with abnormal laboratory	Safety and tolerability of ORIC-533	36 months
Secondary	Maximum plasma concentration (Cmax)	PK of ORIC-533	28 Days
Secondary	Area under the curve last concentration (AUClast)	PK of ORIC-533	28 Days
Secondary	Elimination half-life (t1/2)	PK of ORIC-533	28 Days