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- Klinische proef NCT02556463
A Study of MEDI9197 in Subjects With Solid Tumors or CTCL and in Combination With Durvalumab and/or Palliative Radiation in Subjects With Solid Tumors
A Phase I, First-Time-in-Human Study of MEDI9197, a TLR 7/8 Agonist, Administered Intratumorally as a Single Agent in Subjects With Solid Tumors or CTCL and in Combination With Durvalumab and/or Palliative Radiation in Subjects With Solid Tumors
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Inschrijving (Werkelijk)
Fase
- Fase 1
Contacten en locaties
Studie Locaties
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Ontario
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Toronto, Ontario, Canada, M5G 1Z6
- Research Site
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Villejuif, Frankrijk, 94805
- Research Site
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California
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San Francisco, California, Verenigde Staten, 94115
- Research Site
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Colorado
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Aurora, Colorado, Verenigde Staten, 80045
- Research Site
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Minnesota
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Minneapolis, Minnesota, Verenigde Staten, 55455
- Research Site
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Missouri
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Saint Louis, Missouri, Verenigde Staten, 63110
- Research Site
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New York
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New York, New York, Verenigde Staten, 10029
- Research Site
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North Carolina
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Chapel Hill, North Carolina, Verenigde Staten, 27599-7305
- Research Site
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Pennsylvania
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Philadelphia, Pennsylvania, Verenigde Staten, 19104
- Research Site
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Texas
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Houston, Texas, Verenigde Staten, 77030
- Research Site
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria for All Subjects (Parts 1, 2 and 3)
- Written informed consent and any locally required authorizations.
- Male and female subjects at least 18 years at the time of screening.
- Adequate organ function within 14 days of enrollment confirmed by laboratory results.
- Systemic corticosteroids at doses exceeding 12 mg/day prednisone or equivalent.
- ECOG 0 or 1.
- Highly effective method of contraception from the date of the screening pregnancy test, and continued precautions for 6 months after the final dose of investigational product.
- Baseline Child-Pugh Score of A1 to B7.
- Life expectancy ≥ 12 weeks, as estimated by Royal Marsden Hospital Score of 0 or 1 at baseline.
Subjects with hepatocellular carcinoma (HCC) are eligible if the tumor is defined as nodular type 1 or 2 only.
Additional Inclusion Criteria for Subjects in Parts 1 and 3
- Metastatic/locally advanced solid tumor malignancy that has progressed on, is refractory to, or for which there is no standard of care therapy.
- For subjects with cutaneous/subcutaneous lesions, subjects must have more than one measurable target lesion, at baseline, with a minimum of one lesion that meets protocol specified criteria.
For subjects with deep-seated lesions, subjects must have more than one measurable target lesion at baseline (RECIST v1.1), with a minimum of one deep-seated lesion suitable for image-guided injection and that meets protocol specified criteria.
Additional Inclusion Criteria for Subjects in Part 2 (Closed to Enrollment as of Protocol Amendment 6)
- Clinical diagnosis of CTCL, including documentation of a skin biopsy with histological findings consistent with CTCL or unconfirmed diagnosis of CTCL with confirmation biopsy at screening.
- Stage IB, IIA, or IIB disease: T1, T2 or T3 (patches, plaques or tumors) with measurable lesions.
- Previous treatment with at least one standard therapy used to treat the stage of disease at study entry; Stage IB, IIA or IIB CTCL.
- Measurable skin disease with at least 2 lesions amenable to response assessment.
- At least one lesion must be amenable to injection, ie, ≥ 1.5 cm in the longest diameter.
Exclusion Criteria:
Any of the following would exclude the subject from participation in the study:
- Subjects who have received prior immunotherapy [(including but not limited to CTLA-4, oncolytic virus, oncolytic peptide-all require 100 day washout), programmed death ligand (PDL)-1, or programmed cell death 1 antagonists-both require 14 day washout)] are NOT permitted to enroll, with protocol exceptions.
- Pregnant or lactating.
- Active bacterial, fungal, or viral infections, including chronic or active hepatitis B, chronic or active hepatitis C, or active hepatitis A. Prior documented infections must have resolved.
- Active or prior documented autoimmune or inflammatory disorders, with exceptions per protocol. Includes known allergy to sesame oil and/or nuts.
- Immune-deficiency states - myelodysplastic disorders, marrow failures, human immunodeficiency virus (HIV) infection, history of solid organ transplant or bone marrow allograft, or recent pregnancy.
- Requires continuous (daily) anticoagulation or antiplatelet therapy (including anti aggregants), acetylsalicylic acid (ASA) or nonsteroidal anti-inflammatory drugs (NSAIDs).
- History of coagulopathy resulting in uncontrolled bleeding or other bleeding disorders.
- Rapidly progressing disease per protocol.
- Untreated or uncontrolled central nervous system (CNS) involvement.
- Any concurrent chemotherapy, immunotherapy, or biologic or hormonal therapy for cancer treatment; with exceptions per protocol.
- Unresolved toxicities from prior anticancer therapy, defined as having not resolved to NCI CTCAE v4.03 Grade 0 or 1, with exception of alopecia, vitiligo.
- Uncontrolled concurrent illness.
- Cardiac exclusions: New York Heart Association Class 3 or 4 congestive heart failure, uncontrolled hypertension, acute coronary syndrome within 6 months, clinical important cardiac arrhythmia, mean QTC interval corrected for heart rate >500ms.
- Major surgery within 4 weeks prior to study entry or still recovering from prior surgery.
- Receipt of live, attenuated vaccine within 28 days prior to study entry.
- Receipt of any systemic anticancer therapy not mentioned above within the last 2 weeks or 5 half-lives.
- Cognitive disorder such that informed consent cannot be obtained directly from the subject
- Subjects who have previously participated in this study and received MEDI9197, or concurrent enrollment in another clinical study involving an investigational treatment.
- Subjects who have received prior TLR agonists, both systemic and topical.
- Patients who have received prior therapeutic radiation within 28 days of dosing. All toxicities from prior radiotherapy must have resolved to ≤ Grade 1 or baseline prior to dosing.
- Body weight < 35 kg
- Subjects enrolling in Part 3 (ie, receiving durvalumab) must not have a history of interstitial lung disease or pneumonitis.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Escalation MEDI9197
MEDI9197
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
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Experimenteel: Escalation MEDI9197 with durvalumab
MEDI9197 in combination with durvalumab
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
Subjects will receive durvalumab every 4 weeks
Andere namen:
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Experimenteel: Escalation MEDI9197 durvalumab radiation
MEDI9197 in combination with durvalumab and palliative radiation
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
Subjects will receive durvalumab every 4 weeks
Andere namen:
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Experimenteel: MEDI9197 with palliative radiation
MEDI9197 in combination with palliative radiation
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Safety and tolerability as determined by assessment of dose limiting toxicities and the maximum tolerated dose or maximal assessed dose per protocol of MEDI9197 when administered by intratumoral injection to subjects with solid tumor cancers
Tijdsspanne: From time of informed consent through 4 weeks after last dose of investigational product
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The primary endpoint will be the number (%) of subjects with dose-limiting toxicities, adverse and serious adverse events and other safety parameters.
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From time of informed consent through 4 weeks after last dose of investigational product
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Safety and tolerability as determined by assessment of dose limiting toxicities and the maximum tolerated dose or maximal assessed dose per protocol of MEDI9197 when administered by intratumoral injection to subjects with CTCL
Tijdsspanne: From time of informed consent through 6 months after last dose of investigational product
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The primary endpoint will be the number (%) of subjects with dose-limiting toxicities, adverse and serious adverse events and other safety parameters.
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From time of informed consent through 6 months after last dose of investigational product
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Safety & tolerability as determined by dose limiting toxicities and maximum tolerated or assessed dose of MEDI9197 administered by IT injection in combo with durvalumab and durvalumab plus palliative radiation to subjects with solid tumor cancers.
Tijdsspanne: From time of informed consent through 90 days after last dose of investigational product
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The primary endpoint will be the number (%) of subjects with dose-limiting toxicities, adverse and serious adverse events and other safety parameters.
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From time of informed consent through 90 days after last dose of investigational product
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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The maximum concentration of MEDI9197 after the first injection
Tijdsspanne: Pre-dose to 24 hours post first dose
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Pre-dose to 24 hours post first dose
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The apparent terminal half-life of MEDI9197
Tijdsspanne: Pre-dose to 24 hours post first dose
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Pre-dose to 24 hours post first dose
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Percent change from baseline in cluster of differentiation 8 tumor infiltrating lymphocytes in tumor tissue
Tijdsspanne: Baseline to Day 50
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Baseline to Day 50
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Percent change from baseline in serum inflammatory cytokine levels
Tijdsspanne: Pre-dose to end of study, up to 24 months
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Pre-dose to end of study, up to 24 months
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Percent change from baseline in tumor measurements
Tijdsspanne: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Objective response rate
Tijdsspanne: Pre-dose to end of study, up to 24 months
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Pre-dose to end of study, up to 24 months
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Duration of response
Tijdsspanne: Pre-dose to end of study, up to 24 months
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Pre-dose to end of study, up to 24 months
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Percent change from baseline in CAILDS for subjects with CTCL
Tijdsspanne: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Percent change from baseline in mSWAT scored for subjects with CTCL
Tijdsspanne: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Percent change from baseline in Investigator Global Assessment (IGA) for subjects with CTCL
Tijdsspanne: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Percent change from baseline in Subject Global Assessment (SGA) for subjects with CTCL
Tijdsspanne: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Medewerkers en onderzoekers
Sponsor
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- D6410C00001
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