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Verified by the innovator, on Apr 2022

Technology name

Last update: Jul 2026

Long-Acting Injectable Solid Drug Nanoparticle (SDN) Platform

Sponsor(s)

export_notes
Verified by the innovator, on Apr 2022

Type of technology

Aqueous drug particle suspension

Administration route

Development state and regulatory approval

Active Pharmaceutical Ingredient (API)

Rifapentine

Development Stage

Pre-clinical

Regulatory Approval

Not provided

Description

The use of particle processing technology to generate long-acting injectable nanoparticle formulations for long-acting delivery.

Developer(s)

Tandem Nano
Originator
United Kingdom

Tandem Nano

A University of Liverpool based start-up company using proprietary technology for the generation of novel nanoparticle formulations to improve the delivery of poorly water soluble APIs.

University of Liverpool
Originator

University of Liverpool

Centre for Excellence of Long-acting Therapeutics
Originator

Centre for Excellence of Long-acting Therapeutics

Technology highlight

The generation of high drug-loading nanoparticles with prolonged release for poorly water-soluble drugs with the potential for co-formulation strategies.

Illustration(s)

Technology main components

Active pharmaceutical ingredients, FDA/CDER listed excipients.

Safety, Efficacy and Evidence Summary

Safety

To be determined

Efficacy

Not provided

Evidence Summary

Not provided

References and relevant studies

Not provided

APIs compatibility profile

API desired features
Water-insoluble molecules

Unit: mg/mL
To be determined.

Small molecules

Multiple.

Additional solubility data

None.

Additional stability data

-

API loading: Maximum drug quantity to be loaded

75-90 wt%

API co-administration

2 different APIs : API dependent.

LogP

Not provided

Scale-up and manufacturing prospects

Scale-up prospects

To be determined

Tentative equipment list for manufacturing

To be determined

Manufacturing

To be determined

Specific analytical instrument required for characterization of formulation

To be determined

Excipients & delivery device(s)

Proprietary excipients used

No proprietary excipient used

Novel excipients or existing excipients at a concentration above Inactive Ingredient Database (IID) for the specified route of administration

No novel excipient or existing excipient used

Residual solvents used

No residual solvent used

Delivery device(s)

No delivery device

Additional features

Other features of the technology

Not provided

Release properties

To be determined

Injectability

To be determined

Stability

To be determined

Storage conditions and cold-chain related features

To be determined

Therapeutic area(s)

  • Disease agnostic
Use case(s)

Not provided

Potential associated API(s)

Use of technology

Ease of administration
  • Administered by a community health worker
  • Administered by a nurse
  • Administered by a specialty health worker
  • Self-administered
Frequency of administration

Daily

User acceptance
Not provided

Targeted user groups

Age Cohort
  • Adults
Genders
  • All
  • Male
  • Female
  • Cisgender female
  • Cisgender male
  • Transgender female
  • Transgender male
  • Intersex
  • Gender non-binary
Pregnant individuals

Unspecified

Lactating individuals

Unspecified

Healthy individuals

Unspecified

Comment

Not provided

Rifapentine

Class(es)

Not provided

Development stage

Pre-clinical

Clinical trial(s)

Not provided

Foreseen/approved indication(s)

Not provided

Foreseen user group

Not provided

Foreseen duration between application(s)

Not provided

Applications to Stringent Regulatory Authorities (SRA) / regulatory approvals

Not provided

Class(es)

Not provided

Development stage

Pre-clinical

Clinical trial(s)

Not provided

Foreseen/approved indication(s)

Not provided

Foreseen user group

Not provided

Foreseen duration between application(s)

Not provided

Applications to Stringent Regulatory Authorities (SRA) / regulatory approvals

Not provided

Class(es)

Not provided

Development stage

Not provided

Clinical trial(s)

Not provided

Foreseen/approved indication(s)

Not provided

Foreseen user group

Not provided

Foreseen duration between application(s)

Not provided

Applications to Stringent Regulatory Authorities (SRA) / regulatory approvals

Not provided

Class(es)

Not provided

Development stage

Not provided

Clinical trial(s)

Not provided

Foreseen/approved indication(s)

Not provided

Foreseen user group

Not provided

Foreseen duration between application(s)

Not provided

Applications to Stringent Regulatory Authorities (SRA) / regulatory approvals

Not provided

Partnerships

No partner indicated

All sponsors

Additional information

No.