PEP08
DrugPEP08 is an oral, potent, MTA-cooperative PRMT5 inhibitor.
NCT Number: NCT06973863
This is a first-in-human clinical study of PEP08, a novel cancer therapy being evaluated both as monotherapy and in combination with other treatments in patients with advanced or metastatic solid tumors harboring MTAP deletion.
The study will be conducted in three parts, with Part 1 currently open for enrollment.
The primary objectives of the study are to:
* Evaluate the safety and tolerability of PEP08, PK and PD * Determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) * Assess preliminary signs of anti-tumor activity of PEP08
Key study questions include:
* What is the recommended dose of PEP08 for further development? * Wht is the tolerable dose of PEP08 when administered alone or in combination? * Does PEP08 show early evidence of clinical activity in patients with MTAP-deleted tumors?
Participants in the study will:
* Receive PEP08 alone or in combination with another anti-cancer agent, depending on the study part * Attend regular clinic visits for treatment administration, laboratory assessments, and tumor evaluations * Be enrolled in one of the following study phases over time: * - Part 1: Monotherapy dose escalation (currently enrolling). * - Parts 2 and 3 (monotherapy extension and combination therapy) will be activated in future protocol amendments.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
Westmead Hospital, Wentworthville, New South Wales, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
PEP08 is an oral, potent, MTA-cooperative PRMT5 inhibitor.
Time frame: Up to 2 years
Time frame: Up to 2 years
Time frame: 21 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Time frame: Up to 6 days
Time frame: Up to 2 years
Contact information is provided by the study sponsor or research team.
PharmaEngine
Industry
A Phase 1a/1b Study Evaluating the Clinical Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Anti-tumor Efficacy of PEP08 as Monotherapy and Combination Therapy in MTAP-Del Advanced or Metastatic Solid Tumors
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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