Recruiting
Phase 1

RH324

Sponsor:

ReHeva Biosciences,Inc.

Code:

NCT05580172

Conditions

Safety Issues

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

RH324

Study Details

Brief summary:

Phase 1 open label dose ranging study of RH324 in advanced non-small cell lung cancer

Conditions

Safety Issues

Study ID

NCT05580172

Start date

Jun 1, 2022

Status verified date

Oct, 2022

Completion date

Jan 1, 2025

Anticipated

Primary completion date

Jun 1, 2024

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Advanced Non-Small Cell Lung Cancer
  • Measurable Target Lesion by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1
  • Failed all standard of care including chemotherapy, targeted therapy, and immunotherapy
  • Adults over 18 years
  • Performance status (Eastern Cooperative Oncology Group) less than or equal to 2
  • Life expectancy greater than 2 months
  • Laboratory Values:

Hemoglobin greater than or equal to 9; neutrophils greater than 1,000; platelets greater than 50,000 Liver function tests less than or equal to twice upper limit of normal Serum Creatinine less than or equal to 2 Creatinine clearance greater than or equal to 30 mL per minute Hemoglobin A1C less than 7 Normal Thyroid function

  • No history of hyperthyroidism
  • Abstinence from alcohol and supplements
  • Not pregnant, lactating and willing to use birth control throughout study
  • Able to provide consent
  • Positive Emission Tomography/Computer Tomography part of subjects care plan at baseline

Exclusion Criteria:

  • Prior use of Withania somnifera
  • Phenylketonuria
  • Inability to swallow capsules
  • Hypersensitivity to study drug ingredients
  • Unstable medical or surgical condition
  • History of additional cardiac risk factors
  • Requiring drugs that are "strong" inhibitors of cytochrome P450
  • Requiring irradiation
  • Requiring intravenous fluids or hyperalimentation
  • Requiring transfusions, dialysis, or other procedures
  • Active infection
  • Human Immunodeficiency Virus
  • Must exceed washout period of prior treatments
  • Psychiatric, neurological or other reason that precludes subjects ability to participate

Study Design

Enrollment

6 participants

Anticipated

Allocation

Non randomized

Intervention Model

Sequential

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: Dose Level 1

RH324

experimental: Dose Level 2

RH324

experimental: Dose Level 3

RH324

Interventions

RH324

polymolecular

Primary outcome measure

  • Incidence of Adverse Events Per Common Terminology Criteria for Adverse Events Version 5 [ Time Frame: Through Study Completion 28 Days ]

Central Contacts and Locations

Central contacts

Locations

Case Comprehensive Cancer Center University Hospitals

Recruiting

Cleveland, Ohio, United States, 44106

Contacts

More Information

Sponsor

ReHeva Biosciences,Inc.

Last update posted

Oct 17, 2022

Last verified

Oct, 2022

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by ReHeva Biosciences,Inc. on 2022-10-17.