A First-in-Human Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of KUP-101A in Patients With Selected Advanced Solid Tumors

Recruiting Phase 1 Interventional Study
Cutaneous Melanoma Mucosal Melanoma Cutaneous Squamous Cell Carcinoma (CSCC) Merkel Cell Carcinoma of Skin Basal Cell Carcinoma of Skin
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
21 (estimated)
Sponsor
Kupando GmbH · Industry
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About This Trial

The purpose of this trial is to find the maximum tolerated and recommended Phase 2 dose of KUP-101A and to evaluate its safety and tolerability. Additionally, pharmacokinetics and pharmacodynamics will be assessed, and first data on KUP-101A's efficacy in patients with advanced solid tumors will be obtained.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Histologically confirmed cancer with evidence of advanced disease for which no other standard treatment is available * ECOG Performance status of 0 to 2 * Adequate hematological, renal, and hepatic organ function Exclusion Criteria: * Previous systemic treatment with TLR ago…
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Clinical Operations

+49 30 52 00 58 60 20

clinicaltrials@kupando.com

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