bêta
IA Trial Radar
L'essai clinique NCT06014086 pour Carcinome épidermoïde de la peau, Malignant Melanoma of Skin, Carcinome à cellules de Merkel de la peau est en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici.
Un essai clinique correspond aux filtres sélectionnés
Vue en carte

Intratumoral PH-762 pour carcinome cutané

En recrutement
Les détails de l'essai clinique sont principalement disponibles en anglais. Cependant, l'IA Trial Radar peut vous aider ! Cliquez simplement sur 'Expliquer l'essai' pour voir et discuter des informations sur l'essai dans la langue sélectionnée.
L'essai clinique NCT06014086 est conçu pour étudier le treatment de Carcinome épidermoïde de la peau, Malignant Melanoma of Skin, Carcinome à cellules de Merkel de la peau. Il s'agit d'un essai interventionnel en Phase I. Son statut actuel est : en recrutement. L'essai a débuté le 7 novembre 2023 et vise à recruter 30 participants. Dirigé par Phio Pharmaceuticals, l'essai devrait être terminé d'ici le 1 avril 2026. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 31 juillet 2025.
Résumé succinct
The goal of this clinical trial is to evaluate the safety and tolerability of intratumoral injections of PH-762 in squamous cell carcinoma, melanoma, or Merkel cell carcinomas of the skin, to understand what the body does to the PH-762, and to observe how the tumor responds to the drug. Participants will receive four injections of PH-762 at weekly intervals, into a single tumor, followed by surgical removal of the tumor approximately two weeks later.
Description détaillée
PH-762 is a potent RNAi molecule targeting PD-1. PH-762 can inhibit the immune checkpoint PD-1 in the tumor and thereby impede tumor growth. As a preoperative therapy, it may decrease the lesion size and has the potential to improve surgical morbidity. Intratumoral immunotherapy aims to use the tumor as a 'self-vaccine'. The local immune stimulation can induce robust priming of an anti-tumor immune response while generating systemic (abscopal) tumor responses, mediated by properly activated anti-tumor immune cells in the circulation. Local delivery of immunotherapy is expected to minimize systemic exposure and off-target toxicities.

This is a non-comparative study of neoadjuvant monotherapy using PD-1 targeting self-delivering RNAi (PH-762) in adult subjects with cutaneous squamous cell carcinoma, melanoma, or Merkel cell carcinoma. The study treatment consists of four intratumoral injections of PH-762 at weekly intervals, into a single tumor lesion. Excision of the tumor will occur approximately two weeks following the fourth dose of IT PH-762, and the subjects will be followed for an additional 11 weeks.

Titre officiel

Dose Escalation Study of Neoadjuvant Intratumoral PH-762 for Cutaneous Squamous Cell Carcinoma, Melanoma, or Merkel Cell Carcinoma

Conditions
Carcinome épidermoïde de la peauMalignant Melanoma of SkinCarcinome à cellules de Merkel de la peau
Publications
Articles scientifiques et travaux de recherche publiés sur cet essai clinique:
Autres identifiants de l'essai
  • PHIO-762-2301
Numéro NCT
Date de début (réel)
2023-11-07
Dernière mise à jour publiée
2025-07-31
Date de fin (estimée)
2026-04
Inscription (estimée)
30
Type d'essai
Interventionnel
PHASE
Phase I
Statut
En recrutement
Objectif principal
Traitement
Plan d'attribution
N/A
Modèle d'intervention
Groupe unique
Masquage
Aucun (ouvert)
Bras / Interventions
Groupe de participants/BrasIntervention/Traitement
ExpérimentalSequential escalating doses of PH-762.
Escalating doses of PH-762 are to be tested, with an observation period between doses.
PH-762
PH-762 is a potent RNAi molecule targeting PD-1.
Critère principal d'évaluation
Critères d'évaluationDescription de critèresPériode
Adverse Events
Incidence, severity, seriousness and relatedness of all treatment-emergent adverse events.
16 weeks
Critère secondaire d'évaluation
Critères d'évaluationDescription de critèresPériode
Pharmacokinetics: maximum plasma concentration (Cmax)
Maximum concentration of PH-762 following intratumoral injection.
3.5 weeks
Pharmacokinetics: time to maximum plasma concentration (Tmax)
Time to maximum concentration of PH-762 following intratumoral injection.
3.5 weeks
Pharmacokinetics: area under the curve to last quantifiable plasma concentration (AUClast)
Exposure to PH-762 through last quantifiable concentration following intratumoral injection.
3.5 weeks
Pathologic response
Pathological response will be assessed by relative amount of viable tumor in resection specimens of the treated lesion.
5 weeks
Tumor burden
Change in tumor burden will be assessed per RECIST/ iRECIST guidelines for the treated lesion.
5 weeks
Critères d'éligibilité

Âges éligibles
Adulte, Adulte âgé
Âge minimum
18 Years
Sexes éligibles
Tous
  • Histologically confirmed cutaneous squamous cell carcinoma (cSCC), melanoma, or Merkel cell carcinoma, meeting one of the following criteria:

    • cSCC, resectable local tumors: must be Stage II or lower, amenable to curative resection and in a location where acceptable surgical margins are anticipated
    • cSCC, unresectable local tumors: must be Stage II or lower, tumor has been unresponsive to prior radiation therapy or is not a candidate for curative radiation therapy
    • cSCC, metastatic disease: disease has progressed during or following prior checkpoint inhibitor therapy (anti-PD-1 or anti-PD-L1 antibody)
    • Melanoma, metastatic disease: Stage IV disease with a cutaneous lesion that has progressed during or following checkpoint inhibitor therapy (anti-PD-1/-PD-L1), and if BRAF-mutation is present, has progressed during or following prior treatment with anti-BRAF + MEK therapy
    • Merkel cell carcinoma, metastatic disease: Stage IV disease with a cutaneous lesion that has progressed during or following checkpoint inhibitor therapy (anti-PD-1/PD-L1)
  • A minimum of one tumor of ≥ 1.0 cm and < 3.0 cm in longest dimension that is accessible (with or without imaging guidance) for intratumoral injection and for biopsy and surgical excision must be present. The tumor is not necrotic, hemorrhagic, or friable, and is not within 2 cm of the eye or within 0.5 cm of or on the lip (including the vermilion border) and is not in a mucosal or visceral location.

  • Other malignancy within prior 3 years, with certain exceptions.
  • Current cancer chemotherapy, radiation therapy, immunotherapy, or biologic therapy.
  • Any serious or uncontrolled medical disorder including auto-immune disease that may increase the risk associated with study participation or study drug administration, or interfere with the interpretation of study results.
  • Females who are pregnant or are breastfeeding.
Prosoft Clinical logoProsoft Clinical
Contact central de l'essai
Contact: Linda Mahoney, 508-929-3601, [email protected]
Contact: Mary C Spellman, MD, [email protected]
5 Centres de l'essai dans 1 pays

Arizona

Banner MD Anderson Cancer Center, Gilbert, Arizona, 85234, United States
Mark I Gimbel, MD, Contact, 480-256-6444
En recrutement

California

Paradigm Clinical Research, San Diego, California, 92108, United States
Jamie, Research Coordinator, Contact, 858-274-4226
En recrutement

Florida

Integrity Research, Delray Beach, Florida, 33445, United States
Research Coordinator, Contact, 561-935-9865
En recrutement

Nevada

Skin Cancer and Dermatology Institute, Reno, Nevada, 89509, United States
Jennifer, Research Coordinator, Contact, 775-336-3665
En recrutement

Ohio

Centricity Research, Columbus, Ohio, 43213, United States
Research Coordinator, Contact, 614-336-7880
En recrutement