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Prophylaxis of Complications of Basic Therapy Using Naderin in Socially Significant Diseases (NADERIN-SSD)

26 juin 2026 mis à jour par: MIPO Clinic

Prophylaxis of Complications of Basic Therapy and Medical Rehabilitation Using Naderin in Socially Significant Diseases, Including Malignant Neoplasms, Tuberculosis, and Hepatitis C

This interventional study evaluated the efficacy of Naderin (sodium nucleinate) for the prophylaxis of complications during basic therapy and medical rehabilitation in patients with socially significant diseases, including malignant neoplasms, tuberculosis, and hepatitis C. The study assessed the immunocorrective effects of Naderin on hematological parameters, the incidence of infectious complications, and clinical outcomes.

A total of 75 patients (40 in the main group and 35 in the control group) were enrolled. Patients in the main group received Naderin as an adjunct to standard therapy, while the control group received standard therapy without immunocorrection. The study demonstrated that Naderin reduced the duration of neutropenia by 4-5 days, attenuated the decline in white blood cell and lymphocyte counts during chemotherapy, and reduced the incidence of treatment interruptions due to complications. These findings suggest that Naderin may serve as an effective immunomodulatory agent for supportive care in patients with socially significant diseases.

Aperçu de l'étude

Description détaillée

Rationale Standard treatments for malignant neoplasms, tuberculosis, and hepatitis C may be associated with clinically important complications (e.g., cytopenias, immunosuppression, infections) that can impair treatment delivery and rehabilitation. Naderin (sodium nucleinate) was evaluated as an adjunct immunomodulatory/supportive-care approach intended to improve tolerance of basic therapy and reduce complication-related disruptions.

Study Design and Setting This was a prospective, controlled, open-label interventional study conducted at clinical sites affiliated with the Kazakh National Medical University (KazNMU), Almaty, Kazakhstan, supported by KazNMU Grant 2013. Allocation to intervention vs control was non-randomized (controlled cohort comparison).

Study Population and Groups (high-level)

A total of 75 participants with one of the following diagnostic categories were enrolled: malignant neoplasms, tuberculosis, or hepatitis C. Participants were assigned to:

  • Intervention group: standard-of-care therapy for the underlying condition plus Naderin (immunocorrection).
  • Control group: standard-of-care therapy without Naderin. (Condition-specific eligibility criteria and any stratification by disease category should be presented in the Eligibility Criteria and Study Design/Arms sections rather than repeated here.) Intervention (high-level description) Participants in the intervention group received Naderin (sodium nucleinate) as an adjunct to standard therapy. Key intervention specifications should be captured in the Arms/Interventions module (and/or here if not elsewhere): route, dose, frequency, timing relative to basic therapy, duration, and criteria for dose modification/discontinuation, consistent with protocol reporting standards for reproducibility 1.

Assessments and Follow-up

Participants underwent baseline and follow-up assessments during the active treatment/rehabilitation period that included:

  • Hematology monitoring (e.g., WBC and lymphocyte counts; other CBC indices as applicable to the disease group and therapy).
  • Clinical surveillance for infectious complications using predefined clinical criteria and documentation of antimicrobial treatment/hospitalization where relevant.
  • Documentation of basic-therapy delivery (e.g., interruptions, delays, or discontinuation attributable to complications).
  • Safety monitoring for adverse events temporally associated with adjunctive Naderin and with underlying disease therapy.

Outcomes (high-level; details elsewhere) The study evaluated hematologic parameters, infectious complications, treatment delivery disruption due to complications, and rehabilitation-related clinical outcomes. Outcome definitions, metrics, and time frames should be specified in the dedicated Outcome Measures section per SPIRIT guidance 1 and SPIRIT-Outcomes extension expectations for prespecification 2.

Statistical Approach (high-level) Between-group comparisons were planned using appropriate tests based on outcome type (categorical vs continuous) with a prespecified two-sided significance threshold. If subgroup analyses by disease category (neoplasm vs TB vs HCV) were planned, the analysis set and handling of multiplicity should be stated in the Statistical Analysis Plan or briefly here with a reference, consistent with SPIRIT expectations 1.

Ethics and Oversight The study received ethics approval from the Local Ethics Committee of KazNMU (Approval No. 15678). Written informed consent was obtained prior to enrollment. No data monitoring committee was constituted.

Type d'étude

Interventionnel

Inscription (Réel)

75

Phase

  • Phase 2
  • Phase 3

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Diagnosis of malignant neoplasm, tuberculosis, or hepatitis C (confirmed by clinical, laboratory, and/or histopathological criteria)
  • Age between 18 and 50 years at the time of enrollment
  • Receiving standard basic therapy (chemotherapy, anti-tuberculosis therapy, or antiviral therapy) according to national clinical protocols
  • Signed informed consent to participate in the study
  • Willingness to comply with study procedures and follow-up visits
  • ECOG performance status ≤ 2 or equivalent

Exclusion Criteria:

  • Severe concomitant diseases (e.g., decompensated cardiovascular, renal, or hepatic failure) that could interfere with study participation or outcome assessment
  • Known hypersensitivity or contraindications to Naderin (sodium nucleinate) or its components
  • Pregnancy or lactation
  • Participation in any other interventional clinical trial within 30 days prior to enrollment
  • Active or uncontrolled infections (other than the primary study condition)
  • Severe immunodeficiency (e.g., HIV/AIDS, advanced hematological malignancies) not related to the primary study condition
  • Mental or cognitive impairment that would preclude informed consent or compliance with study procedures
  • History of organ transplantation requiring immunosuppressive therapy
  • Any other condition that, in the investigator's opinion, would make the participant unsuitable for the study

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Soins de soutien
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Naderin + Standard Therapy
Participants received standard basic therapy for their underlying disease (malignant neoplasms, tuberculosis, or hepatitis C) in combination with Naderin (sodium nucleinate) as an adjunct immunocorrective therapy for the prophylaxis of complications.
Naderin (sodium nucleinate) is an immunomodulatory agent administered as an adjunct to standard basic therapy for the prophylaxis of complications. It enhances immune function, reduces the duration of neutropenia, and attenuates the decline in hematological parameters during chemotherapy and other aggressive therapies.
Autres noms:
  • nucléinate de sodium
Comparateur actif: Standard Therapy Alone
Participants received standard basic therapy for their underlying disease (malignant neoplasms, tuberculosis, or hepatitis C) without immunocorrection.
Standard basic therapy according to clinical protocols for malignant neoplasms, tuberculosis, and hepatitis C. Includes chemotherapy, anti-tuberculosis therapy, and antiviral therapy as per national guidelines.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Incidence of Infectious Complications
Délai: Up to 6 months (from study start to completion)
The number and proportion of participants who developed infectious complications (e.g., pneumonia, febrile neutropenia, bacterial infections) during the course of basic therapy (chemotherapy, anti-tuberculosis therapy, antiviral therapy).
Up to 6 months (from study start to completion)
Duration of Neutropenia
Délai: Up to 6 months (from study start to completion)
The number of days participants experienced neutropenia (absolute neutrophil count < 1.0 × 10⁹/L) during the course of basic therapy.
Up to 6 months (from study start to completion)
Change in White Blood Cell (WBC) and Lymphocyte Counts
Délai: Baseline and up to 6 months
The change in white blood cell count (× 10⁹/L) and lymphocyte count (× 10⁹/L) from baseline to post-treatment assessment, comparing the Naderin group and control group.
Baseline and up to 6 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Time to Recovery of Hematological Parameters
Délai: Up to 6 months
The number of days required for normalization of white blood cell count, lymphocyte count, and absolute neutrophil count after the completion of therapy.
Up to 6 months
Adverse Events Profile
Délai: Up to 6 months
The number and severity of adverse events (graded according to CTCAE criteria) experienced by participants in both groups.
Up to 6 months
Duration of Hospitalization
Délai: Up to 6 months
The total number of days participants were hospitalized during the course of therapy and follow-up
Up to 6 months

Collaborateurs et enquêteurs

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Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

15 mai 2013

Achèvement primaire (Réel)

21 septembre 2013

Achèvement de l'étude (Réel)

12 mars 2014

Dates d'inscription aux études

Première soumission

22 juin 2026

Première soumission répondant aux critères de contrôle qualité

22 juin 2026

Première publication (Réel)

26 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

26 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

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Informations sur les médicaments et les dispositifs, documents d'étude

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Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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