RVU120 in Patients With Acute Myeloid Leukemia or High-risk Myelodysplastic Syndrome

Phase 1

Active, not recruiting

• Conditions: Acute Myeloid Leukemia; High-risk Myelodysplastic Syndrome
• Interventions: Drug: RVU120(SEL120)

• Registration Number: NCT04021368
• Lead Sponsor: Ryvu Therapeutics SA

Brief Summary

This first-in-human study will evaluate RVU120 (SEL120), a novel small molecule CDK8/19 inhibitor, in patients with Acute Myeloid Leukemia (AML) or High-risk Myelodysplastic Syndrome (HR-MDS), in terms of selection of the recommended dose for further clinical development and assessment of safety, tolerability, preliminary anti-leukemic activity, as well as pharmacokinetic and pharmacodynamic profiles.

Detailed Description

The study will determine the recommended phase II dose (RP2D) and safety of RVU120 (SEL120) given as monotherapy over a range of dose-levels, following a closely controlled dose escalation study design.

Study Timeline

• Study First Submitted: 2019-07-12
• Study First Submitted QC: 2019-07-15
• Study First Posted: 2019-07-16
• Study Start: 2019-09-04
• Status Verified: 2024-01
• Last Update Submitted: 2024-02-13
• Last Update Posted: 2024-02-14
• Primary Completion: 2024-12-30
• Study Completion: 2024-12-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 112

Inclusion Criteria

All the following criteria must be met for a patient to be eligible for the study:

1. Written informed consent provided prior to any study-related procedure.
2. Age ≥18 years.
3. AML diagnosis according to the 2016 World Health Organisation (WHO) classification (Arber et al. 2016) with relapsed or refractory disease with no available therapy who have exhausted the applicable standard of care; or Myelodysplastic Syndrome (MDS) diagnosis according to the 2016 WHO classification (Arber et al. 2016) with high-risk disease per the Revised International Prognostic Scoring System (IPSS-R >4.5) and with relapsed or refractory disease with no available therapy who have exhausted the applicable standard of care.
4. Eastern Cooperative Oncology Group (ECOG) performance score of 0-2.
5. Patients must have been off anti-cancer treatment prior to study.
6. Patients must have recovered from the toxic effects of previous treatments.
7. Peripheral white blood cell (WBC) count <10x10^9/L; Platelet count >10,000/μL; Serum albumin ≥ 30g/L (3.0g/dL); Normal coagulation (elevated INR, prothrombin time or APTT <1.3 x ULN acceptable); AST and ALT ≤3x ULN; Total bilirubin ≤1.5 x ULN; Creatinine clearance ≥60 mL/min (Cockcroft-Gault formula);
8. Adequate cardiac function
9. Life expectancy of at least 12 weeks.
10. For females of childbearing potential (FCBP), a negative pregnancy test must be confirmed before enrolment. FCBP must commit to use a highly effective method of contraception during study participation and until 6 months after the last dose of study drug. Females must also refrain from donating blood or egg (ovum) during the same time period.
11. For males, an effective barrier method of contraception must be used during study participation until 6 months after the last dose of study drug, if the patient is sexually active with a FCBP. Males must also refrain from donating blood or sperm during the same time-period.
12. Investigator considers the patient to be suitable for participation in the clinical study

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Exclusion Criteria

1. Active central nervous system (CNS) leukemia.
2. Previous treatment with CDK8-targeted therapy.
3. Patients who have undergone major surgery within 28 days prior to first dose of study drug.
4. Hematopoietic stem cell transplant within 120 days prior to first dose of study drug.
5. Active acute graft versus host disease (GVHD)
6. Infections and acute inflammatory conditions
7. Known seropositivity or history of HIV
8. Known positive test of / or known active diagnosis of COVID-19 viral infection
9. Ongoing significant liver disease
10. Impairment of gastrointestinal function or gastrointestinal disease
11. Ongoing drug-induced pneumonitis.
12. Concurrent participation in another investigational clinical trial.
13. Taking any medications, herbal supplements or other substances (including smoking) that are known to be strong inhibitors or inducers of CYP1A2 or that can prolong Q wave to T wave (QT) interval and/or cause torsade de pointes within less than 5 half-lives, prior to first dose of study drug.
14. Significant cardiac dysfunction or poorly controlled angina.
15. Currently taking drugs that are documented, in the drug package insert, to have a risk of causing prolonged QTc or torsades de pointes (TdP) within 5 half-lives prior to first dose of study drug.
16. Personal or family history of serious ventricular arrhythmia, or QT interval corrected for heart rate (QTc) ≥470 ms (Bazett's formula).
17. Any other prior or current medical condition or extenuating circumstance that, in the Investigator's opinion, could jeopardize patient safety or interfere with the objectives of the study.
18. Prior history of malignancies other than AML or MDS, unless the patient has been free of the disease for 5 years or more prior to Screening.
19. Pregnant or breast-feeding females.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
RVU120(SEL120)	RVU120(SEL120)	The first part of the study consists of dose-escalation cohorts where patients will receive ascending doses of RVU120(SEL120) to determine the recommended dose (RD) for further clinical development. The second part of the study is an enrichment cohort where additional 6 to 20 patients will be treated with RVU120(SEL120) to support the evaluation of the RD.

Primary Outcome Measures

Name	Time	Method
Incidence of Adverse Events (Safety and Tolerability)	Up to 2 years	Safety and tolerability profile will be assessed by Common Terminology Criteria for Adverse Events v5.0 and summarized by type, frequency, and severity of adverse events.
Recommended dose (RD)	Up to 2 years	The RD will be determined using all available data, which will include dose limiting toxicities (DLTs) and other toxicities, signs of anti-leukemic activity, pharmacokinetic and pharmacodynamic characteristics.

Secondary Outcome Measures

Name	Time	Method
The Maximum Observed Concentration (C[max])	Up to 2 years	Pharmacokinetic profile of RVU120(SEL120) will be characterized using the Maximum Observed Concentration (C\[max\]).
The Terminal Half-life (t[1/2])	Up to 2 years	Pharmacokinetic profile of RVU120(SEL120) will be characterized using the Terminal Half-life (t\[1/2\]).
The Area Under the Curve (AUC)	Up to 2 years	Pharmacokinetic profile of RVU120(SEL120) will be characterized using the Area Under the Curve (AUC).
The Volume of Distribution at Steady State (Vss)	Up to 2 years	Pharmacokinetic profile of RVU120(SEL120) will be characterized using the Volume of Distribution at Steady State (Vss).
Anti-leukemic activity	Up to 2 years	Anti-leukemic activity will be assessed by AML or MDS Response Criteria (Döhner et al., 2017, or Cheson et al., 2006, respectively).

Trial Locations

Locations (10)

Sylvester Comprehensive Cancer Center, University of Miami Hospital and Clinics; 🇺🇸 Miami, Florida, United States

Northside Hospital; 🇺🇸 Atlanta, Georgia, United States

MD Anderson Cancer Center; 🇺🇸 Houston, Texas, United States

Tennessee Oncology; 🇺🇸 Nashville, Tennessee, United States

MICS Centrum Medyczne Toruń; 🇵🇱 Toruń, Poland

Uniwersyteckie Centrum Kliniczne; 🇵🇱 Gdańsk, Poland

Instytut Hematologii i Transfuzjologii; 🇵🇱 Warsaw, Poland

Dolnośląskie Centrum Onkologii, Pulmonologii i Hematologii; 🇵🇱 Wrocław, Poland

Świętokrzyskie Centrum Onkologii, Klinika Hematologii i Transplantacji Szpiku; 🇵🇱 Kielce, Świętokrzyskie, Poland

Washington University School of Medicine; 🇺🇸 Saint Louis, Missouri, United States