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.
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
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.
- Conditions
- Snake Bites, Antivenins, Snake Venoms
- 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 group | Role | What they receive |
|---|---|---|
| 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. 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.
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)
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
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
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.
- First posted31 Oct 2017
- Study start17 Oct 2019
- Primary completion14 Sep 2021
- Study completion14 Sep 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Snake BitesStudies of the same condition, open and under way.
- More trials run by Institut PasteurThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Institut Pasteur
- Sponsor type
- Industry (pharma, biotech, devices)
- 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
- Investigators
- Armand Nkwescheu, MD, Principal investigator, Cameroon Society of Epidemiology, CameroonYap Boum, MD, Principal investigator, Médecins Sans Frontière
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 40720423Benhammou 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 38668590Chippaux 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
Study at a glance
From the registry record, last updated by the sponsor on 22 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Anti-venoms Serum in Africa (ESAA). Data Collection in Real Life Conditions
- ClinicalTrials.gov ID
- NCT03326492
- Acronym / sponsor ID
- ESAA / 2016-092
- Conditions
- Snake Bites, Antivenins, Snake Venoms
- Keywords
- Snake bites, Antivenom serum, Snake venoms
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 474 participants (actual)
- Lead sponsor
- Institut PasteurIndustry (pharma, biotech, devices)
- Collaborators
- Cameroon Society of Epidemiology (CaSE), Centre International de Recherches d'Enseignements et de Soins (CIRES), Centre Pasteur du Cameroun, Inosan Biopharma
- Study start
- 17 Oct 2019 (actual)
- Primary completion
- 14 Sep 2021 (actual)
- Study completion
- 14 Sep 2021 (actual)
- First posted
- 31 Oct 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients bitten by a snake | – | Drug: Antivenom serum Inoserp Pan-Africa® injectionAny 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. |
Who may qualify
- Ages
- 5 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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
Key inclusion criteria (2 listed)
- 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
Key exclusion criteria (4 listed)
- Patient refusal
- Under 5 year-old
- Antivenom serum administration before the arrival in the participating center
- History of severe allergic reactions to antivenom serum
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Antivenom serum Inoserp Pan-Africa® injectionParticipation 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. | Drug | Patients bitten by a snake |
Primary outcome
Short term tolerance of the antivenom serum Inoserp Pan-Africa®
Time frame: 30 months
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
3 secondary outcomes
Short term efficacy of the antivenom serum Inoserp Pan-Africa®
Time frame: 30 months
Medium term tolerance of the antivenom serum Inoserp Pan-Africa®
Time frame: 30 months
Medium term efficacy of the antivenom serum Inoserp Pan-Africa®
Time frame: 30 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Sep 2025.
- Background: PubMed 40720423Chippaux 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.
- Results publication: PubMed 38668590Benhammou 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.
- Results publication: PubMed 37939111Chippaux 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.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Armand Nkwescheu, MD principal investigator
Cameroon Society of Epidemiology, Cameroon
Yap Boum, MD principal investigator
Médecins Sans Frontière
13 sites in 1 country: see every site and its status.
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.