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CompletedNCT03326492ESAAUpdated Sep 22, 2025

Evaluation of Anti-venoms Serum in Africa

An observational study in Snake Bites, Antivenins and Snake Venoms, sponsored by Institut Pasteur. Completed at 13 sites in Cameroon. Open to participants aged 5 Years and older. Per ClinicalTrials.gov, last updated 2025-09-22.

Sponsored by Institut Pasteur · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
474
Ages
5 Years and older
Sex
All
01

Study summary

There is little or no assessment under real-use conditions of the efficacy and the tolerance in the short, medium and long term of the antivenoms currently on the market and used in the treatment of snake bites.

The main objective is to assess the short term tolerance (\< 2 hours post-injection) of the antivenom Inoserp Pan-Africa® (temporary market authorization) from Inosan laboratory currently available in Cameroon.

Read the detailed description

Globally, the number of annual envenomings is estimated to be between 420,000 and 1,800,000. In sub-Saharan Africa, the annual number of envenomings is estimated at 315,000, leading to more than 9,000 amputations and about 7,000 deaths.

Snake bites are recognized by many authors as a neglected disease, whose incidence is underestimated or even unknown in several countries of sub-Saharan Africa. Few data are currently available on the morbidity, mortality and economic impact of snake bites.

In Cameroon and particularly in the northern part of the country, where the density of snakes is high, a few studies have been carried out. In 2002, the annual incidence of envenomings was estimated at 200/100 000 inhabitants, of which 85% was due to Echis ocellatus, and the lethality was 23.9% in some centers. The Ministry of Public Health introduced snake bites in 2015 as a priority health problem in the list of diseases being monitored. Thus, a national epidemiological surveillance system, with a weekly count of snake bites, has been implemented. In the first year, the incidence of annual snake bites was 11.4/100,000 inhabitants, representing more than 2,500 bites per year, including 43 deaths and a case fatality rate of up to 6% in some areas. The northern region (Adamaoua, North and Far North regions) (savanna and mixed zone) accounts for 40% of the country's burden and 77% of the deadly burden, while the forest zone accounts for 32% of the burden Morbid disease and 16% of the fatal burden (ministerial source). The monitoring is based on paper registers for bite reporting, supplemented by the sending of pharmacovigilance data by text messages, but this is very little used in current practice. The data collection system in Cameroon could therefore be improved in terms of both completeness and speed of centralizing data.

These estimates are likely to be well below the reality given the non-exhaustive nature of the data collection and the frequent use of traditional practitioners without referral in a hospital structure.

In recent years, FAV-Afrique® produced by Sanofi-Pasteur was the treatment of reference for venomous snake bites in West and Central Africa. It was the most evaluated and the most effective, reducing by a factor 5 to 10 the mortality. This anti-venom serum was polyspecific, containing an antivenom against ten species of snakes: Naja melanoleuca, nigricollis \& haje; Dendroaspis polylepis, viridis \& jamesoni, Bitis gabonica \& arietans; Echis leucogaster \& ocellatus.

However, Sanofi-Pasteur stopped production (last batch produced in January 2014 and expired in June 2016), making it necessary to use other snake antivenoms. Since the end of 2015, two new antivenoms are available in Cameroon where they are granted a provisional marketing authorization. Few clinical trials have evaluated the antivenoms currently available in Africa.

Some clinical efficacy and safety data have been published for Inoserp Pan-Africa®. However, the number of subjects was limited and assessment was limited to the period of hospitalization.

The lack of sufficient data on incidence and mortality associated with snake bites, the current weakness of the epidemiological data collection system and the presence on the market of antivenoms that are very little evaluated in terms of tolerance, effectiveness make action necessary.

The main objective of the study is therefore to assess the tolerance and the efficacy of the antivenom Inoserp Pan-Africa® from Inosan laboratory currently available in Cameroon.This study will be conducted under routine conditions in order to avoid bias in the results through the implementation of dedicated logistics which would not be representative of the usual conditions.

02

Conditions studied

  • Snake Bites
  • Antivenins
  • Snake Venoms

Browse trials for

Keywords

  • Snake bites
  • Antivenom serum
  • Snake venoms
03

In context

Snake Bites

38 studies on the registry are indexed under Snake Bites; 11 are open to participants now.

This study's enrollment of 474 is above the median of 99 across 19 observational studies indexed under Snake Bites.

Browse Snake Bites studies →

Lead sponsor

Institut Pasteur is the lead sponsor of 99 studies on the registry; 41 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Any patient over 5 years old (inclusive) visiting at a participating center for curative care following a snake bite, with or without confirmed envenoming, will be proposed to participate in the study

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Any patient over 5 years old (inclusive) visiting at a participating center for a snake bite with or without confirmed envenoming
  • to research

Exclusion criteria

Exclusion Criteria:

  • Patient refusal
  • Under 5 year-old
  • Antivenom serum administration before the arrival in the participating center
  • History of severe allergic reactions to antivenom serum
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
474 participants (actual)
Patient registry
No

Groups and cohorts

  • Patients bitten by a snake

    Any patient over 5 years old going to a participating center for curative care following a snake bite. Participation to the study does not change usual follow-up of patients. Antivenom serum Inoserp Pan-Africa® injection will be decided according to the clinical evaluation of the patient.

    Drug: Antivenom serum Inoserp Pan-Africa® injection

Interventions

  • DrugAntivenom serum Inoserp Pan-Africa® injection

    Participation to the study does not change usual follow-up of patients. All medical procedures will be performed and products will be used in a routine manner. Antivenom serum Inoserp Pan-Africa® injection will be decided according to the clinical evaluation of the patient.

06

What researchers measure

Primary outcomes

  1. Short term tolerance of the antivenom serum Inoserp Pan-Africa®

    The short-term tolerance of the antivenom serum Inoserp Pan-Africa® will be assessed by the monitoring of the clinical signs occurence less than 2 hours post-injection

    Time frame: 30 months

Secondary outcomes

  1. Short term efficacy of the antivenom serum Inoserp Pan-Africa®

    The short-term efficacy of the antivenom serum Inoserp Pan-Africa® will be assessed by the clinical evaluation when the patient arrives at the hospital and then regularly until 48 hours post-injection

    Time frame: 30 months

  2. Medium term tolerance of the antivenom serum Inoserp Pan-Africa®

    The medium term tolerance of the antivenom serum Inoserp Pan-Africa® will be assessed by the monitoring of the clinical signs occurence more than 72 hours post-injection

    Time frame: 30 months

  3. Medium term efficacy of the antivenom serum Inoserp Pan-Africa®

    The medium term efficacy of the antivenom serum Inoserp Pan-Africa® will be assessed by the vital status at 15 days of any patient who received at least one dose of the antivenom serum and by the reported consequences 15 days after the first dose administration of the antivenom serum

    Time frame: 30 months

07

Study locations

13 sites
  • Hôpital de District d'Akonolinga
    Akonolinga, Cameroon
  • Hôpital régional de Buea
    Buea, Cameroon
  • Hôpital de District de Guider
    Guider, Cameroon
  • Hôpital de District de Kolofata
    Kolofata, Cameroon
  • Hôpital Régional de Limbe
    Limbe, Cameroon
  • Hôpital de District de Mora
    Mora, Cameroon
  • Hôpital Norvégien de N'Gaoundéré
    N'Gaoundéré, Cameroon
  • Hôpital Régional de N'Gaoundéré
    N'Gaoundéré, Cameroon
  • Hôpital Saint Malte de Njombe
    Njombé, Cameroon
  • Hôpital de District de Poli
    Poli, Cameroon
  • Hôpital de District de Sa'a
    Sa'a, Cameroon
  • Hôpital de District de Tokombere
    Tokonbéré, Cameroon
  • Centre des Urgences de Yaounde (CURY)
    Yaoundé, Cameroon
08

References and documents

Publications

  • Chippaux JP, Amta P, Madec Y, Ntone R, Noel G, Clauteaux P, Boum Ii Y, Nkwescheu AS, Taieb F. Epidemiologic, clinical, and therapeutic aspects of formally identified Echis romani bites in northern Cameroon. PLoS Negl Trop Dis. 2025 Jul 28;19(7):e0013195. doi: 10.1371/journal.pntd.0013195. eCollection 2025 Jul. PubMed 40720423 ↗
  • Benhammou D, Chippaux JP, Ntone R, Madec Y, Amta P, Noel G, Karl FN, Perilhou A, Matchim L, Sanchez M, Ndifon M, Clauteaux P, Eteki L, Boum Y 2nd, Nkwescheu AS, Taieb F. Snakebites in Cameroon: Tolerance of a Snake Antivenom (Inoserp PAN-AFRICA) in Africa in Real-Life Conditions. Toxins (Basel). 2024 Mar 22;16(4):165. doi: 10.3390/toxins16040165. PubMed 38668590 ↗
  • Chippaux JP, Ntone R, Benhammou D, Madec Y, Noel G, Perilhou A, Karl F, Amta P, Sanchez M, Matchim L, Clauteaux P, Eteki L, Ndifon M, Boum Y, Nkwescheu AS, Taieb F. Real life condition evaluation of Inoserp PAN-AFRICA antivenom effectiveness in Cameroon. PLoS Negl Trop Dis. 2023 Nov 8;17(11):e0011707. doi: 10.1371/journal.pntd.0011707. eCollection 2023 Nov. PubMed 37939111 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03326492
Lead sponsor
Institut Pasteur
Collaborators
Cameroon Society of Epidemiology (CaSE), Centre International de Recherches d'Enseignements et de Soins (CIRES), Centre Pasteur du Cameroun, Inosan Biopharma
Responsible party
Sponsor
First posted
Oct 31, 2017
Start date
Oct 17, 2019
Primary completion
Sep 14, 2021
Completion
Sep 14, 2021
Last update
Sep 22, 2025

Study contacts

Armand Nkwescheu, MD
principal investigator · Cameroon Society of Epidemiology, Cameroon
Yap Boum, MD
principal investigator · Médecins Sans Frontière

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.

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Discussion

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