Intratumoral Injection of IP-001 Following Thermal Ablation in Patients With CRC, NSCLC, and STS

Colon Cancer Clinical Trial

— INJECTABL-1  

Official title:

Intratumoral Injection of IP-001 Following Thermal Ablation in Patients With Advanced Solid Tumors. A Multicenter Phase 1b/2a Trial in Colorectal Cancer, Non-small Cell Lung Cancer, and Soft Tissue Sarcoma Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05688280
• Other study ID #: IP-IIO-622
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: November 29, 2022
• Est. completion date: May 2024

Study information

• Verified date: December 2023
• Source: Immunophotonics, Inc.
• Contact: Jane Bierman
• Phone: +31 64 523 4949
• Email: jane.bierman2[@]iqvia.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical trial is to determine the safety and efficacy of IP-001 for intratumoral injection administration following thermal ablation of a solid tumor.

Description:

The therapeutic approach taken by this clinical trial may offer patients a therapeutic benefit after failure of standard chemotherapy and immunotherapy. Patients giving written informed consent will undergo screening during the Pretreatment Period to determine eligibility for trial entry. The Pretreatment Period will include collection and recording of medical history, concomitant medications, baseline symptoms, previous therapies, and baseline assessments. The patient's baseline tumor burden will be recorded with radiological assessments, along with analyzing location and size of tumors to identify and characterize target tumor(s) that will be treated and/or followed during the clinical trial. If confirmed eligible for the study, the patient will advance into the Treatment Period. During the Treatment Period, patients will receive a routine radiofrequency ablation (RFA), followed by an injection of investigational product (IP-001 for Injection) into the tumor. Patients can be treated every 6 weeks for up to 4 treatments with RFA + IP-001 for Injection. A patient will move to the 6-month Follow-up Period when the patient has completed 4 treatment cycles or if the decision is made that no subsequent treatments will be administered. During the Follow-up Period, there will be a Follow-up Visit every 6 weeks for 5 visits, at disease progression, or prior to the start of a new antineoplastic treatment.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 44
• Est. completion date: May 2024
• Est. primary completion date: May 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Stage 3 or Stage 4 CRC, NSCLC, or STS who have failed, are ineligible, refused, or become intolerant to at least first line (but no more than 4 lines) of systemic therapy

2. Life expectancy of > 6 months. Only have lesions with the longest diameter of = 5 cm.

3. Presence of at least one non-bone tumor lesion that is ablation-accessible, with a minimum size of 1.0 cm.

4. Measurable disease according to RECIST 1.1.

5. Age = 18 years.

6. ECOG performance status 0-1.

7. Bone marrow function: neutrophil count = 1.5 × 109/L, platelet count = 100 × 109/L, hemoglobin = 90 g/L.

8. Adequate hematological function defined by white blood cell count = 2.5 × 109/L with absolute neutrophil count = 1.5 × 109/L, and hemoglobin = 9 g/dL (transfusions allowed on study).

9. Adequate hepatic function defined by a total bilirubin level = 1.5 × the upper limit of normal (ULN) range and aspartate transaminase (AST) and alanine aminotransferase (ALT) levels = 2.5 × ULN for all patients, or for patients with documented metastatic disease to the liver and AST and ALT levels = 5 × ULN. Patients with documented Gilbert disease are allowed if total bilirubin is less than 3 × ULN.

10. Adequate renal function defined by an estimated creatinine clearance = 50 mL/min according to the Cockcroft-Gault formula (or local institutional standard method).

11. Men and women with childbearing potential agree to use effective contraception. Women of childbearing potential must have a negative pregnancy test (serum) before inclusion.

Exclusion Criteria:

1. Known allergic reaction to shellfish, crabs, crustaceans, or any trial components, used in trial treatment.

2. Malignant primary brain tumors or evidence of brain metastases or leptomeningeal disease.

3. Patients who have received chemotherapy, radiotherapy, immunotherapy, or concurrent or recent treatment with any other investigational agents within 21 days prior to treatment.

4. Patients who have not recovered to common terminology criteria for adverse events (CTCAE) Grade = 1 from all side effects of prior therapies except for residual toxicities.

5. Patients with a history of malignancy, with the exception of non-melanoma skin cancers and in situ cancers.

6. Concomitant treatment with systemic corticosteroids (10 mg prednisolone or equivalent) or other immunosuppressive therapy.

7. Anti-coagulation therapies which cannot be stopped 24 hours prior to trial treatment.

8. Severe or uncontrolled cardiovascular disease (congestive heart failure New York Heart Association classification III or IV).

9. Documented HIV positive.

10. Active Hepatitis C or Hepatitis B Viral infection.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Colon Cancer
• Lung Neoplasms
• Metastatic Solid Tumor
• Nonsmall Cell Lung Cancer
• Sarcoma
• Soft Tissue Sarcoma

Intervention

Drug:
• 1.0% IP-001 for Injection
4 mL 1.0% IP-001 for Injection following RFA every 6 weeks for up to 4 treatments.

Locations

Country	Name	City	State
France	Institut Bergonie	Bordeaux
France	Hospitalier Pitie-Salpetriere	Paris
France	Hôpital Foch	Suresnes
France	Institut Gustave Roussy	Villejuif
Germany	Johann Wolfgang Goethe-Univresitat Frankfurt/Main	Frankfurt
Germany	SLK-Kliniken Heilbronn GmbH	Heilbronn
Germany	Munchen Klinik Bogenhausen	Munich
Switzerland	IOSI Ospedale San Giovanni Bellinzona	Bellinzona
Switzerland	Inselspital Universitatsspital, Bern	Bern
Switzerland	Kantonsspital Graubunden	Chur
Switzerland	Kantonsspital St. Gallen	St. Gallen
United Kingdom	University College London Hospitals	London
United Kingdom	Churchill Hospital	Oxford
United States	Miami Cardiac & Vascular Institute	Coral Gables	Florida
United States	University of Louisville Physicians, PSC	Louisville	Kentucky
United States	Stephenson Cancer Center	Oklahoma City	Oklahoma

Sponsors (1)

Lead Sponsor	Collaborator
Immunophotonics, Inc.

Countries where clinical trial is conducted

United States,  France,  Germany,  Switzerland,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and Tolerability	The assessment of safety will be based on incidence of adverse events.	Up to 12 weeks
Secondary	Efficacy: Disease control according to Immune Response Evaluation Criteria in Solid Tumors for immune-based treatment (iRECIST) (iDC)	An iDC is defined as any complete response (CR or iCR), partial response (PR or iPR), or stable disease (SD or iSD) for 12 weeks according to iRECIST achieved during the trial until disease progression according to iRECIST, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Disease control according to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) (DC)	A DC is defined as any complete response (CR), partial response (PR) or stable disease (SD) for 12 weeks from start of treatment according to RECIST 1.1 achieved during trial until disease progression according to iRECEST, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Objective response according to iRECIST (iOR)	An iOR is defined as any complete response (CR or iCR) or partial response (PR or iPR) according to iRECIST achieved during the trial until disease progression according to iRECIST, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Duration of response according to iRECIST (iDOR)	An iDOR is defined as the time from the first documentation of iOR until disease progression according to iRECIST (iPD) or death from any cause. iPD is defined as the time point of first iUPD without subsequent iSD, iPR or iCR before trial discontinuation.	Up to 12 weeks
Secondary	Efficacy: Progression-free survival according to iRECIST (iPFS)	An iPFS is defined as the time from treatment start until disease progression according to iRECIST (iPD) or death from any cause, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Objective response according to RECIST 1.1 (OR)	An OR is defined as any complete response (CR) or partial response (PR) according to RECIST 1.1 achieved during trial until disease progression, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Duration of response according to RECIST 1.1 (DOR)	A DOR is defined as the time from the first documentation of OR until disease progression according to RECIST 1.1, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Progression-free survival according to RECIST 1.1 (PFS)	A PFS is defined as the time from treatment start until disease progression according to RECIST 1.1, or death from any cause, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Time to response according to iRECIST 1.1 (iTTR)	An iTTR is defined as the time from start of trial treatment until iOR according to iRECIST achieved during the trial.	Up to 12 weeks
Secondary	Efficacy: Time to response according to RECIST 1.1 (TTR)	A TTR is defined as the time from treatment start until OR according to iRECIST achieved during the trial.	Up to 12 weeks
Secondary	Efficacy: Disease-free survival (DFS)	A DFS is defined as the time from start of treatment that the patient survives without any signs or symptoms of cancer or death from any cause, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: Overall survival (OS)	An OS is defined as the time from start of treatment until death from any cause.	Up to 12 weeks
Secondary	Efficacy: OR of the injected lesions according to RECIST 1.1	An OR of the ablated and injected (treated) lesions will be assessed using RECIST 1.1.	Up to 12 weeks
Secondary	Efficacy: OR of the non-injected lesions according to RECIST 1.1	An OR of the non-ablated and non-injected (untreated) lesions will be assessed using the RECIST 1.1 until disease progression according to RECIST 1.1, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: iOR of the injected lesions according to iRECIST	An iOR of the ablated and injected (treated) lesions will be assessed using the iRECIST until disease progression according to RECIST 1.1, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks
Secondary	Efficacy: iOR of the non-injected lesions according to iRECIST	An iOR of the non-ablated and non-injected (untreated) lesions will be assessed using the iRECIST until disease progression according to RECIST 1.1, death from any cause, or start of a subsequent anticancer treatment, whichever occurs first.	Up to 12 weeks