IBOV 204,302.33 ▼ 0.74% IPSA 10,999.64 ▼ 1.47% IPC MEX 64,460.91 ▼ 1.30% MERVAL 2,824,123 ▼ 2.51% COLCAP 2,534.92 ▼ 2.09% BVL PERÚ 60,766.81 ▼ 1.71% USD/BRL5.02▲ 0.80% USD/MXN17.97▼ 0.07% USD/CLP978.61▲ 0.60% USD/COP3,240▲ 0.99% USD/PEN3.44▼ 0.06% USD/ARS1,517▼ 0.24% USD/UYU40.09▲ 2.39% USD/PYG5,835▲ 3.05% USD/BOB11.87▲ 2.15% USD/DOP60.29▲ 3.70% USD/CRC453.46▲ 2.32% USD/GTQ7.64▲ 3.39% USD/HNL26.86▲ 0.86% USD/NIO36.62▲ 0.26% USD/VES871.68▼ 0.13% USD/PAB1.00— 0.00% USD/BZD2.00— 0.00% USD/JMD 157.28 — 0.00% USD/TTD6.70▲ 2.23% EUR/BRL5.62▲ 0.33% BRENT 88.88 ▼ 0.03% WTI 83.11 ▼ 0.11% IRON ORE 161.91 — — COPPER 6.61 ▲ 0.03% GOLD 4,461 ▲ 1.78% SILVER 65.59 ▲ 1.26% SOY 1,184 ▲ 3.20% CORN 480.50 ▲ 10.02% WHEAT 655.00 ▲ 3.93% COFFEE 317.25 ▼ 5.51% SUGAR 16.43 ▼ 1.79% ORANGE JUICE 138.55 ▼ 0.47% COTTON 85.03 ▲ 2.33% COCOA 5,719 ▲ 3.18% BEEF 223.60 ▼ 3.93% CATTLE 339.10 ▼ 3.16% LITHIUM 75.20 ▲ 1.47% PETR4 41.64 ▼ 0.05% VALE3 72.97 ▲ 0.83% ITUB4 38.60 ▼ 1.03% BBDC4 16.85 ▲ 0.36% ABEV3 14.89 ▼ 0.80% BBAS3 19.37 ▲ 0.47% B3SA3 14.26 ▼ 0.21% WEGE3 47.59 ▲ 0.49% PRIO3 59.14 ▼ 0.19% SUZB3 41.33 ▲ 2.35% RENT3 34.68 ▼ 0.09% AZZA3 15.89 ▼ 2.63% CSAN3 3.22 ▼ 1.83% RAIZ4 0.25 — 0.00% PCAR3 2.75 ▼ 0.36% GMAT3 3.65 ▼ 1.08% PSSA3 48.13 ▼ 0.54% CVCB3 1.33 ▼ 2.92% POSI3 3.36 ▲ 2.44% SLCE3 13.34 ▲ 0.30% NATU3 8.14 ▼ 0.73% IBOV 204,302.33 ▼ 0.74% IPSA 10,999.64 ▼ 1.47% IPC MEX 64,460.91 ▼ 1.30% MERVAL 2,824,123 ▼ 2.51% COLCAP 2,534.92 ▼ 2.09% BVL PERÚ 60,766.81 ▼ 1.71% USD/BRL 5.16 ▲ 0.01% USD/MXN 17.06 ▼ 0.24% USD/CLP 913.98 ▲ 0.04% USD/COP 3,140 ▲ 0.03% USD/PEN 3.36 ▼ 0.66% USD/ARS 1,493 ▲ 0.10% USD/UYU 40.27 ▲ 1.24% USD/PYG 5,939 ▲ 1.68% USD/BOB 11.64 ▼ 0.76% USD/DOP 58.34 ▲ 1.25% USD/CRC 445.92 ▲ 0.89% USD/GTQ 7.62 ▲ 2.21% USD/HNL 26.79 ▲ 1.57% USD/NIO 36.62 ▲ 0.69% USD/VES 762.44 ▼ 0.13% USD/PAB 1.00 — 0.00% USD/BZD 2.00 — 0.00% USD/JMD 157.28 — 0.00% USD/TTD 6.70 ▲ 0.61% EUR/BRL 5.95 ▲ 1.01% BRENT 88.88 ▼ 0.03% WTI 83.11 ▼ 0.11% IRON ORE 161.91 — — COPPER 6.61 ▲ 0.03% GOLD 4,461 ▲ 1.78% SILVER 65.59 ▲ 1.26% SOY 1,184 ▲ 3.20% CORN 480.50 ▲ 10.02% WHEAT 655.00 ▲ 3.93% COFFEE 317.25 ▼ 5.51% SUGAR 16.43 ▼ 1.79% ORANGE JUICE 138.55 ▼ 0.47% COTTON 85.03 ▲ 2.33% COCOA 5,719 ▲ 3.18% BEEF 223.60 ▼ 3.93% CATTLE 339.10 ▼ 3.16% LITHIUM 75.20 ▲ 1.47% PETR4 41.64 ▼ 0.05% VALE3 72.97 ▲ 0.83% ITUB4 38.60 ▼ 1.03% BBDC4 16.85 ▲ 0.36% ABEV3 14.89 ▼ 0.80% BBAS3 19.37 ▲ 0.47% B3SA3 14.26 ▼ 0.21% WEGE3 47.59 ▲ 0.49% PRIO3 59.14 ▼ 0.19% SUZB3 41.33 ▲ 2.35% RENT3 34.68 ▼ 0.09% AZZA3 15.89 ▼ 2.63% CSAN3 3.22 ▼ 1.83% RAIZ4 0.25 — 0.00% PCAR3 2.75 ▼ 0.36% GMAT3 3.65 ▼ 1.08% PSSA3 48.13 ▼ 0.54% CVCB3 1.33 ▼ 2.92% POSI3 3.36 ▲ 2.44% SLCE3 13.34 ▲ 0.30% NATU3 8.14 ▼ 0.73%
since 2009
Wednesday, October 7, 2026

Brazil Healthcare

Brazil Clears Trials of Vivax Malaria Vaccine

By · October 7, 2026 · 4 min read
An Anopheles stephensi mosquito feeding

Health: Brazil

Key Facts

—Who. Brazil’s health regulator Anvisa approved the Vivaxin vaccine, developed by the CTVacinas centre at the Federal University of Minas Gerais (UFMG), the University of São Paulo (USP) and the laboratory Cristália.

—What. Permission for a Phase 1 trial in people. It will test safety and immune response of a vaccine against malaria caused by the Plasmodium vivax parasite.

—Where. Hospital das Clínicas of UFMG in Belo Horizonte, the capital of Minas Gerais state.

—Numbers. 48 healthy adults aged 18 to 59, three doses 28 days apart, followed for 360 days.

—US link. No vaccine against vivax malaria exists for the public anywhere, according to the developers. The two vaccines the World Health Organization recommends target a different parasite, P. falciparum.

—Status. Early-stage human testing only. Nothing here shows yet that the vaccine protects people.

—As of. 8 October 2026, 00:00 GMT.

Brazil’s health regulator Anvisa has cleared the first human trial of Vivaxin, a vaccine against vivax malaria made by Brazilian universities and a Brazilian drug company. The approval was published on Wednesday 7 October 2026. If the vaccine works, it would fill a gap that global malaria programmes have not yet closed.

What We Know

Anvisa approved the clinical development dossier and the clinical research process in Resolution-RE No. 3,956 of 6 October 2026. The approval appeared in the federal official gazette on Wednesday 7 October, according to the CTVacinas centre at UFMG.

The trial will enrol 48 healthy volunteers aged 18 to 59 who have never had malaria. Participants will receive three doses 28 days apart and will be followed for 360 days.

The trial is double-blind, randomised and placebo-controlled, according to the developers. It will run at the clinical research centre of the Hospital das Clínicas of UFMG in Belo Horizonte.

The aim of Phase 1 is to check safety, reactions to the injection and the immune response. The results will guide the later phases needed to show whether the vaccine protects against the disease.

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Why Vivax Malaria Needs Its Own Vaccine

Malaria is caused by several species of parasite spread by mosquitoes. The vaccines the World Health Organization recommends today, RTS,S and R21/Matrix-M, were designed against P. falciparum, the species that dominates in sub-Saharan Africa.

P. vivax caused about 63% of estimated malaria cases in the Americas in 2024, according to the WHO’s World Malaria Report, which is why a Brazilian vaccine matters here. The developers say no vaccine against it is available to the public anywhere in the world.

Vivaxin combines three variants of a parasite surface protein, called PvCSP, in a single molecule. The goal is to block the parasite before it reaches the liver, and in mice the formulation fully prevented infection in some of the animals, according to Brazilian research reports.

Fountains in Praça da Liberdade, Belo Horizonte, Brazil
Praça da Liberdade in Belo Horizonte, the city where the trial will run. Photo: Michelle Tamietti / Wikimedia Commons (CC BY 3.0)
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The Scale of the Problem in Brazil

Brazil recorded 118,037 malaria cases in 2025, and more than 99% of them were in the Amazon region, according to the CTVacinas centre. The disease keeps people from working, said Ricardo Gazzinelli, who coordinates CTVacinas, which is why he sees a large socioeconomic effect.

Public money backs the project. The funders include Brazil’s science ministry, its national science fund, the Finep innovation agency and the Ministry of Health.

What Is Not Known

None of the reports we reviewed gives a start date for recruiting volunteers. They also give no date for results or for a later trial that could test protection.

Mouse results do not predict how people will respond. Many vaccines that work in animals fail in humans, which is why Phase 1 is only the first step.

What It Means for Travelers and US Readers

Nothing changes for travellers soon, because the vaccine is years from any possible approval. Anyone heading to the Amazon should keep following medical advice on malaria prevention.

For US readers, the story is about where tropical-disease research is moving. A vaccine built in Brazil for a parasite that global vaccine makers have largely left alone could matter to health agencies and drug investors who follow malaria.

Frequently Asked Questions

What did Anvisa approve?

Anvisa approved the clinical development dossier and research process for Vivaxin, allowing a Phase 1 trial in people. The approval is in Resolution-RE No. 3,956 of 6 October 2026.

What is vivax malaria?

It is malaria caused by the Plasmodium vivax parasite, spread by mosquitoes. It causes most malaria in the Americas, while the approved vaccines target another species, P. falciparum.

How will the trial work?

It will enrol 48 healthy adults aged 18 to 59 in Belo Horizonte. They will receive three doses 28 days apart and be followed for 360 days.

Is the vaccine available now?

No. Phase 1 only tests safety and immune response, and later trials must show protection before any approval for the public.

Sources

CTVacinas / UFMG · Estado de Minas · O Tempo · ClinicalTrials.gov NCT07172724

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This article was produced by The Rio Times’ automated newsroom system. How we use AI · Report an error · Editorial responsibility: Matthias Camenzind, Editor-in-Chief

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