Study of ORIC-533 in Relapsed or Refractory Multiple Myeloma

  • STATUS
    Recruiting
  • End date
    Jun 23, 2024
  • participants needed
    48
  • sponsor
    Oric Pharmaceuticals
Updated on 23 March 2022

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.

Details
Condition Relapsed or Refractory Multiple Myeloma
Treatment ORIC-533
Clinical Study IdentifierNCT05227144
SponsorOric Pharmaceuticals
Last Modified on23 March 2022

Eligibility

Yes No Not Sure

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 ≥60 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 >50,000/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
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note