Dashboard

To map and track work being done on paediatric innovation, access and delivery, GAP-f has worked with its partners to develop a coherent and end-to-end approach to monitoring priority products through their product life-cycle. This dashboard summarises the current status of investigation, development and introduction of prioritised products, highlighting progress and remaining gaps.

This monitoring effort draws from existing data sources available in the public domain and synthetizes the work undertaken at the different stages of product lifecycle by different GAP-f partners and relevant stakeholders. The dashboard will be periodically reviewed and where a specific monitoring tool or dashboard already exists (such as for TB), the dashboard will direct the user to appropriate web pages.

 

Antibiotics

Priority products

Amoxicillin-clavulanic acid

Azithromycin

Cefiderocol

Nitrofurantoin

Links / Reports

Hepatitis

Priority products

Sofosbuvir 100 mg

Links / Reports

HIV

Priority products

Dolutegravir 10 mg

Prioritization Evaluation

Product Development

WHO has recommended Dolutegravir-based HIV treatment for all children and provided dosing recommendations for children over four weeks of age and more than 3 kg in July 2020. In late 2020, the United States Food and Drug Administration approved one generic version of 10 mg scored dispersible Dolutegravir tablets, further expanding the access of younger children to Dolutegravir, with an additional generic version approved in March 2021.

Regulatory Affairs

Inclusion in 2023 EMLc
Yes
WHO guidelines
Yes

Product Access

Adoption / Procurement / Rollout & Uptake

FDA approval
Yes
EMA approval
Yes
EOI
Yes
WHO Pre-qualification
Yes
Intellectual property barrier Registration status National EMLc Guidelines First order placed Roll out started
Afghanistan
Albania
Algeria
Angola
Antigua and Barbuda
Argentina
Armenia
Aruba
Azerbaijan
Bahamas
Bangladesh
Barbados
Belarus
Belize
Benin
Bhutan
Bolivia (Plurinational State of)
Bosnia and Herzegovina
Botswana
British Virgin Islands
Burkina Faso
Burundi
Cabo Verde
Cambodia
Cameroon
Central African Republic
Chad
Chile
Colombia
Comoros
Congo
Costa Rica
Cote d'Ivoire
Cuba
Democratic People's Republic of Korea
Democratic Republic of the Congo
Djibouti
Dominica
Dominican Republic
Ecuador
Egypt
El Salvador
Equatorial Guinea
Eritrea
Eswatini
Ethiopia
Fiji
Gabon
Gambia
Georgia
Ghana
Grenada
Guatemala
Guinea
Guinea-Bissau
Guyana
Haiti
Honduras
India
Indonesia
Iran (Islamic Republic of)
Iraq
Jamaica
Jordan
Kazakhstan
Kenya
Kiribati
Kosovo
Kyrgyzstan
Lao People's Democratic Republic
Lebanon
Lesotho
Liberia
Libya
Madagascar
Malawi
Malaysia
Maldives
Mali
Marshall Islands
Mauritania
Mauritius
Micronesia (Federated States of)
Mongolia
Montenegro
Morocco
Mozambique
Myanmar
Namibia
Nauru
Nepal
Nicaragua
Niger
Nigeria
Pakistan
Palau
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Republic of Moldova
Rwanda
Saint Kitts and Nevis
Saint Lucia
Saint Vincent and the Grenadines
Samoa
Sao Tome and Principe
Senegal
Serbia
Seychelles
Sierra Leone
Solomon Islands
Somalia
South Africa
South Sudan
Sri Lanka
Sudan
Suriname
Syrian Arab Republic
Tajikistan
Thailand
Timor-Leste
Togo
Tonga
Tunisia
Turkmenistan
Tuvalu
Uganda
Ukraine
United Republic of Tanzania
Uruguay
Uzbekistan
Vanuatu
Venezuela (Bolivarian Republic of)
Viet Nam
Western Sahara
Yemen
Zambia
Zimbabwe

Abacavir/lamivudine/dolutegravir 60/30/5 mg

Darunavir/ritonavir 120/20 mg

Long-acting cabotegravir

TAF-XTC ± DTG

Links / Reports

Neglected Tropical Diseases
* focus on 4 diseases Schistosomiasis, Human African Trypanosomiasis, Scabies and Onchocerciasis, and Visceral Leishmaniasis

Priority products

Acoziborole 320 mg

Amphotericin B

Ivermectin 1 or 1.5 mg

L-praziquantel 150 mg

L-praziquantel 300 mg

Miltefosine 20 mg

Moxidectin

Links / Reports

Therapeutic area Priority products Product life cycle
Antibiotics
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation
Hepatitis
Evaluation
HIV
Prioritization Evaluation

Product Development

WHO has recommended Dolutegravir-based HIV treatment for all children and provided dosing recommendations for children over four weeks of age and more than 3 kg in July 2020. In late 2020, the United States Food and Drug Administration approved one generic version of 10 mg scored dispersible Dolutegravir tablets, further expanding the access of younger children to Dolutegravir, with an additional generic version approved in March 2021.

Regulatory Affairs

Inclusion in 2023 EMLc
Yes
WHO guidelines
Yes

Adoption

FDA approval
Yes
EMA approval
Yes
EOI
Yes
WHO Pre-qualification
Yes
Intellectual property barrier Registration status National EMLc Guidelines First order placed Roll out started
Afghanistan
Albania
Algeria
Angola
Antigua and Barbuda
Argentina
Armenia
Aruba
Azerbaijan
Bahamas
Bangladesh
Barbados
Belarus
Belize
Benin
Bhutan
Bolivia (Plurinational State of)
Bosnia and Herzegovina
Botswana
British Virgin Islands
Burkina Faso
Burundi
Cabo Verde
Cambodia
Cameroon
Central African Republic
Chad
Chile
Colombia
Comoros
Congo
Costa Rica
Cote d'Ivoire
Cuba
Democratic People's Republic of Korea
Democratic Republic of the Congo
Djibouti
Dominica
Dominican Republic
Ecuador
Egypt
El Salvador
Equatorial Guinea
Eritrea
Eswatini
Ethiopia
Fiji
Gabon
Gambia
Georgia
Ghana
Grenada
Guatemala
Guinea
Guinea-Bissau
Guyana
Haiti
Honduras
India
Indonesia
Iran (Islamic Republic of)
Iraq
Jamaica
Jordan
Kazakhstan
Kenya
Kiribati
Kosovo
Kyrgyzstan
Lao People's Democratic Republic
Lebanon
Lesotho
Liberia
Libya
Madagascar
Malawi
Malaysia
Maldives
Mali
Marshall Islands
Mauritania
Mauritius
Micronesia (Federated States of)
Mongolia
Montenegro
Morocco
Mozambique
Myanmar
Namibia
Nauru
Nepal
Nicaragua
Niger
Nigeria
Pakistan
Palau
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Republic of Moldova
Rwanda
Saint Kitts and Nevis
Saint Lucia
Saint Vincent and the Grenadines
Samoa
Sao Tome and Principe
Senegal
Serbia
Seychelles
Sierra Leone
Solomon Islands
Somalia
South Africa
South Sudan
Sri Lanka
Sudan
Suriname
Syrian Arab Republic
Tajikistan
Thailand
Timor-Leste
Togo
Tonga
Tunisia
Turkmenistan
Tuvalu
Uganda
Ukraine
United Republic of Tanzania
Uruguay
Uzbekistan
Vanuatu
Venezuela (Bolivarian Republic of)
Viet Nam
Western Sahara
Yemen
Zambia
Zimbabwe

Procurement

FDA approval
Yes
EMA approval
Yes
EOI
Yes
WHO Pre-qualification
Yes
Intellectual property barrier Registration status National EMLc Guidelines First order placed Roll out started
Afghanistan
Albania
Algeria
Angola
Antigua and Barbuda
Argentina
Armenia
Aruba
Azerbaijan
Bahamas
Bangladesh
Barbados
Belarus
Belize
Benin
Bhutan
Bolivia (Plurinational State of)
Bosnia and Herzegovina
Botswana
British Virgin Islands
Burkina Faso
Burundi
Cabo Verde
Cambodia
Cameroon
Central African Republic
Chad
Chile
Colombia
Comoros
Congo
Costa Rica
Cote d'Ivoire
Cuba
Democratic People's Republic of Korea
Democratic Republic of the Congo
Djibouti
Dominica
Dominican Republic
Ecuador
Egypt
El Salvador
Equatorial Guinea
Eritrea
Eswatini
Ethiopia
Fiji
Gabon
Gambia
Georgia
Ghana
Grenada
Guatemala
Guinea
Guinea-Bissau
Guyana
Haiti
Honduras
India
Indonesia
Iran (Islamic Republic of)
Iraq
Jamaica
Jordan
Kazakhstan
Kenya
Kiribati
Kosovo
Kyrgyzstan
Lao People's Democratic Republic
Lebanon
Lesotho
Liberia
Libya
Madagascar
Malawi
Malaysia
Maldives
Mali
Marshall Islands
Mauritania
Mauritius
Micronesia (Federated States of)
Mongolia
Montenegro
Morocco
Mozambique
Myanmar
Namibia
Nauru
Nepal
Nicaragua
Niger
Nigeria
Pakistan
Palau
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Republic of Moldova
Rwanda
Saint Kitts and Nevis
Saint Lucia
Saint Vincent and the Grenadines
Samoa
Sao Tome and Principe
Senegal
Serbia
Seychelles
Sierra Leone
Solomon Islands
Somalia
South Africa
South Sudan
Sri Lanka
Sudan
Suriname
Syrian Arab Republic
Tajikistan
Thailand
Timor-Leste
Togo
Tonga
Tunisia
Turkmenistan
Tuvalu
Uganda
Ukraine
United Republic of Tanzania
Uruguay
Uzbekistan
Vanuatu
Venezuela (Bolivarian Republic of)
Viet Nam
Western Sahara
Yemen
Zambia
Zimbabwe

Rollout & Uptake

FDA approval
Yes
EMA approval
Yes
EOI
Yes
WHO Pre-qualification
Yes
Intellectual property barrier Registration status National EMLc Guidelines First order placed Roll out started
Afghanistan
Albania
Algeria
Angola
Antigua and Barbuda
Argentina
Armenia
Aruba
Azerbaijan
Bahamas
Bangladesh
Barbados
Belarus
Belize
Benin
Bhutan
Bolivia (Plurinational State of)
Bosnia and Herzegovina
Botswana
British Virgin Islands
Burkina Faso
Burundi
Cabo Verde
Cambodia
Cameroon
Central African Republic
Chad
Chile
Colombia
Comoros
Congo
Costa Rica
Cote d'Ivoire
Cuba
Democratic People's Republic of Korea
Democratic Republic of the Congo
Djibouti
Dominica
Dominican Republic
Ecuador
Egypt
El Salvador
Equatorial Guinea
Eritrea
Eswatini
Ethiopia
Fiji
Gabon
Gambia
Georgia
Ghana
Grenada
Guatemala
Guinea
Guinea-Bissau
Guyana
Haiti
Honduras
India
Indonesia
Iran (Islamic Republic of)
Iraq
Jamaica
Jordan
Kazakhstan
Kenya
Kiribati
Kosovo
Kyrgyzstan
Lao People's Democratic Republic
Lebanon
Lesotho
Liberia
Libya
Madagascar
Malawi
Malaysia
Maldives
Mali
Marshall Islands
Mauritania
Mauritius
Micronesia (Federated States of)
Mongolia
Montenegro
Morocco
Mozambique
Myanmar
Namibia
Nauru
Nepal
Nicaragua
Niger
Nigeria
Pakistan
Palau
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Republic of Moldova
Rwanda
Saint Kitts and Nevis
Saint Lucia
Saint Vincent and the Grenadines
Samoa
Sao Tome and Principe
Senegal
Serbia
Seychelles
Sierra Leone
Solomon Islands
Somalia
South Africa
South Sudan
Sri Lanka
Sudan
Suriname
Syrian Arab Republic
Tajikistan
Thailand
Timor-Leste
Togo
Tonga
Tunisia
Turkmenistan
Tuvalu
Uganda
Ukraine
United Republic of Tanzania
Uruguay
Uzbekistan
Vanuatu
Venezuela (Bolivarian Republic of)
Viet Nam
Western Sahara
Yemen
Zambia
Zimbabwe
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation

Neglected Tropical Diseases
* focus on 4 diseases Schistosomiasis, Human African Trypanosomiasis, Scabies and Onchocerciasis, and Visceral Leishmaniasis

Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation
Prioritization Evaluation