Skip to content

Phase II/III Clinical Study CSF470 Plus BCG Plus GM-CSF vs IFN Alpha 2b in Stage IIB, IIC and III Melanoma Patients

Randomized, Comparative Phase II/III Study Between Treatment With CSF470 Vaccine (Allogeneic, Irradiated) Plus BCG and MOLGRAMOSTIN (rhGM-CSF) as Adjuvants and Interferon-alfa 2b (IFN-ALPHA), in Stages IIB, IIC and III Post Surgery Cutaneous Melanoma Patients

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01729663
Enrollment
108
Registered
2012-11-20
Start date
2009-04-30
Completion date
Unknown
Last updated
2015-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cutaneous Melanoma

Keywords

melanoma, irradiated-allogeneic cells, therapeutic vaccine, Interferon alpha 2-b

Brief summary

Randomized, open, Phase II-III study, comparative between treatment with CSF-470 vaccine , allogeneic, irradiated with BCG and molgramostin (rHuGM-CSF) as adjuvants and interferon alfa 2b (IFN-alpha2b) treatment , in stages IIB, IIC o III (AJCC) post-surgery cutaneous melanoma patients. This study has been approved by ANMAT ( Administración Nacional de Medicamentos, Alimentos y Tecnología Médica (ANMAT)), number 1556/2011 (www.anmat.gov.ar). The study Institution is Instituto Médico Especializado Alexander Fleming, Ciudad Autónoma de Buenos Aires, Argentina. The Sponsor is Laboratory Pablo Cassará (LPC, S.R.L.). Study population include a total of 108 patients (72 patients will receive CSF470 vaccine and 36 patients will receive alpha IFN-alpha 2b) for a total of 24 months. CSF-470 treatment will consist of four vaccine doses id injection (three weeks apart), then one dose every two months for the first year and them every three months for the second year. Each vaccine consist of a mixture of 17,6.106 melanoma cells, from four melanoma cell lines, not genetically modified and lethally irradiated. As adjuvant BCG (120 µg prot) the first day and rHuGM-CSF (Molgramostim, 400 µg, fractionated in four days doses) will be used. IFN-alpha 2b treatment will consist of s.c. injection of 10 million units (MU) (5 t/w ) for four weeks and then 5 MU (3t/w) for 23 months. Both treatments will also compare quality of life (QOL) and study a possible correlation in the CSF470 vaccine arm between the induced immune response and clinical outcome

Interventions

BIOLOGICALCSF470 vaccine, BCG, Molgramostim

Sponsors

Fundacion Sales
CollaboratorUNKNOWN
National Agency for Scientific and Technological Promotion, Argentina
CollaboratorOTHER
Fundacion Cancer FUCA
CollaboratorUNKNOWN
National Council of Scientific and Technical Research, Argentina
CollaboratorOTHER_GOV
Instituto Nacional del Cáncer, Argentina
CollaboratorOTHER_GOV
Laboratorio Pablo Cassará S.R.L.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* histologically confirmed cutaneous melanoma stages IIB, IIC or III (AJCC) * patients non-detectable disease (NED) after surgery as asserted by CAT scans. Melanoma pts with unknown primary tumor site could be included in the study * life expectancy \> 6 months * performance status (ECOG) 0 or 1 * Time post surgery not more than 4 months * no chemotherapy, radiotherapy or any biological treatments prior to this study. * patients must have CATscans of brain, thorax, abdomen and pelvis in the 60 previous days to trial enrolling * To have laboratory studies (no more than 15 days before entering the study) * laboratory eligibility criteria include: hematocrit: ≥35 (hemoglobin \> 10,5 gr %); WBC count \> 3500/mm3, platelets \> 100.000/mm3, total and direct bilirubin, serum oxalacetic transaminase and glutamic pyruvic transaminase \< 1.5 fold the upper normal value; LDH ≤ 450 mU/ml * negative serology for HIV, anti-HCV and HBsAg * serum creatinine \< 2.0 mg % * all patients must give written informed consent before inclusion in the Study.

Exclusion criteria

* Pregnant or breast-feeding women * Diabetes (Type I or II) * Antecedents of psychiatric diseases * Evidence of active infections * Antecedents of viral or autoimmune hepatitis * Previous autoimmune diseases * Morbid Obesity, defined as CMI (Corporal mass index)\>37 kg/m2 in women and \>40 kg/m2 in men. * Other diseases that require treatment with regular corticoids or non steroids anti-inflammatory drugs

Design outcomes

Primary

MeasureTime frameDescription
Efficacytwo yearsOS, DFS, Partial or total remission (PR or CR)
securitytwo yearsmeasured according to the NCI-Common Toxicity Criteria

Secondary

MeasureTime frameDescription
Quality of Lifetwo yearsQOL:evaluated with EORTC QLQ-C30 questionnaire; ECOG Performance status
Induction of immune responsestwo yearsInduction of immune responses associated to different vaccine doses for 2 years (Trial duration) \]Cellular immunity (DTH) - Humoral immunity

Countries

Argentina

Contacts

Primary ContactJosé Mordoh, MD, PhD
jmordoh@alexanderfleming.org54-11-6323-2900
Backup ContactMaría M Barrio, PhD
barrio.marcela@gmail.com54-11-6323-2900

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026