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Snake BitesESAANCT03326492

Evaluation of Anti-venoms Serum in Africa

An observational study of Snake Bites and Antivenins, run by Institut Pasteur at 13 sites in Cameroon.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 5 years and older
Conditions the study is for
Snake Bites, Antivenins, Snake Venoms
What is being tested?
Antivenom serum Inoserp Pan-Africa® injection
Type of treatment
Injection or infusion
How many people
474 participants
Where
13 sitesCameroon
Study dates
17 Oct 2019to 14 Sep 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 5 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

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

Who may be able to join

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

Who cannot join

  • Patient refusal
  • Under 5 year-old
  • Antivenom serum administration before the arrival in the participating center
  • History of severe allergic reactions to antivenom serum

Trial locations and contacts

13 sites in 1 country.

13 sites in 1 country

Cameroon13 sites
  • Hôpital de District d'Akonolinga

    Akonolinga

  • Hôpital régional de Buea

    Buea

  • Hôpital de District de Guider

    Guider

  • Hôpital de District de Kolofata

    Kolofata

  • Hôpital Régional de Limbe

    Limbe

  • Hôpital de District de Mora

    Mora

  • Hôpital Norvégien de N'Gaoundéré

    N'Gaoundéré

  • Hôpital Régional de N'Gaoundéré

    N'Gaoundéré

  • Hôpital Saint Malte de Njombe

    Njombé

  • Hôpital de District de Poli

    Poli

  • Hôpital de District de Sa'a

    Sa'a

  • Hôpital de District de Tokombere

    Tokonbéré

  • Centre des Urgences de Yaounde (CURY)

    Yaoundé

Other trials in Cameroon

About this study

Official title: Evaluation of Anti-venoms Serum in Africa (ESAA). Data Collection in Real Life Conditions

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.

Being tested
Antivenom serum Inoserp Pan-Africa® injection
Keywords
Snake bites, Antivenom serum, Snake venoms
Medical subject headings
Snake Bites

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Antivenom serum Inoserp Pan-Africa® injectionDrug

    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.

Study groups in NCT03326492
Study groupRoleWhat they receive
Patients bitten by a snakeAny 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.
Receives: Drug: Antivenom serum Inoserp Pan-Africa® injection

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

    Measured: 30 months

Secondary outcomes (3)
  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

    Measured: 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

    Measured: 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

    Measured: 30 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Oct 2017
  2. Study start17 Oct 2019
  3. Primary completion14 Sep 2021
  4. Study completion14 Sep 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
474 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03326492
Sponsor's protocol ID
2016-092
Acronym
ESAA
Status last verified
Feb 2022
First submitted
29 Aug 2017
Last updated
22 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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

Questions about this trial

What is this clinical trial studying?

An observational study of Snake Bites and Antivenins, run by Institut Pasteur at 13 sites in Cameroon.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 13 sites in Cameroon. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Short term tolerance of the antivenom serum Inoserp Pan-Africa® (time frame: 30 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03326492, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Sep 2025.

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