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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study to Investigate Safety and Efficacy of KB111 for the Treatment of Hailey-Hailey DiseaseCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hailey-Hailey disease, Skin and Connective Tissue Diseases, hereditary disease, hereditary skin disorder, skin disorder, vesiculobullous skin diseaseRecruitingEarly phase 12026-07-21NCT07717346
A Study Assessing KB407 for the Treatment of Cystic FibrosisCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, cystic fibrosis, hereditary disease, lung disorder, pancreas disorder, respiratory system disorderRecruitingPhase 12026-05-07NCT05504837
A Study Comparing KB803 and Matched Placebo in Patients With Dystrophic Epidermolysis BullosaCollagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Injuries, Craniocerebral Trauma, Eye Injuries, Facial Injuries, Skin Abnormalities, Skin and Connective Tissue Diseases, connective tissue disorder, corneal disorder, epidermolysis bullosa, epidermolysis bullosa dystrophica, eye disorder, hereditary disease, hereditary skin disorder, injury, nervous system disorder, nervous system injury, recessive dystrophic epidermolysis bullosa, skin disorder, vesiculobullous skin diseaseRecruitingPhase 32026-03-12NCT07016750
A Study Comparing KB801 Verse Placebo in Patients With Stage 2 or 3 Neurotrophic Keratitisneurotrophic keratopathyRecruitingPhase 1 / Phase 22026-02-27NCT06999733
A Study Assessing KB707 for the Treatment of Advanced Solid Tumor Malignancies Affecting the LungsNeoplasms by Site, Thoracic Neoplasms, bronchial neoplasm, bronchogenic carcinoma, lung disorder, lung neoplasm, neoplasm, non-small cell lung carcinoma, respiratory system disorder, respiratory tract neoplasmRecruitingPhase 1 / Phase 22025-10-24NCT06228326
A Study of KB408 for the Treatment of Alpha-1 Antitrypsin DeficiencyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Subcutaneous Emphysema, alpha 1-antitrypsin deficiency, hereditary disease, liver disorder, lung disorder, pulmonary emphysema, respiratory system disorderRecruitingPhase 12025-07-22NCT06049082
A Natural History Study of Corneal Abrasions in Patients With Dystrophic Epidermolysis Bullosa (DEB)Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Injuries, Craniocerebral Trauma, Eye Injuries, Facial Injuries, Hallopeau-Siemens Disease, Skin Abnormalities, Skin and Connective Tissue Diseases, connective tissue disorder, corneal disorder, epidermolysis bullosa, epidermolysis bullosa dystrophica, eye disorder, hereditary disease, hereditary skin disorder, injury, nervous system disorder, nervous system injury, skin disorder, vesiculobullous skin diseaseRecruitingNot stated2025-07-02NCT06563414
A Study Assessing KB707 for the Treatment of Locally Advanced or Metastatic Solid TumorsNeoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Skin and Connective Tissue Diseases, cancer, cutaneous melanoma, melanocytic neoplasm, melanoma, neoplasm, neuroendocrine neoplasm, primitive neuroectodermal tumor, skin disorder, skin neoplasmRecruitingPhase 1 / Phase 22025-05-18NCT05970497
A Study Assessing KB304 for the Treatment of Wrinkles in WomenDécolleté Wrinkles; Pigmentation; Wrinkles in DecolletageActive, not recruitingPhase 1 / Phase 22025-05-13NCT06724900
A Phase I Study of KB301, a Replication-Incompetent, Non-Integrating Vector Expressing Human Type III Collagen (COL3) for the Treatment of Superficial Skin DepressionsFine Lines; Skin Roughness; Skin Thickness; WrinkleActive, not recruitingPhase 12025-05-13NCT04540900
Long-Term Follow-up ProtocolCollagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin Abnormalities, Skin and Connective Tissue Diseases, connective tissue disorder, epidermolysis bullosa, epidermolysis bullosa dystrophica, hereditary disease, hereditary skin disorder, recessive dystrophic epidermolysis bullosa, skin disorder, vesiculobullous skin diseaseRecruitingNot stated2021-06-08NCT04917887