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Patient-Led Research Collaborative

Full company profile

uuid0052xv9

Namestring
Patient-Led Research Collaborative
Legal namestring
Patient Led Research Collaborative
Company typeenum
Private
Founded yearstring
-
Descriptiontext

The Patient-Led Research Collaborative (PLRC) is an international non-profit research organization founded in 2020 that focuses on improving research into Long COVID and infection-associated chronic conditions. It is staffed by approximately 10 individuals who themselves live with these conditions and come from diverse professional backgrounds. The organization's stated mission is to advance the breadth, depth, and speed of global research and to advocate for policies that improve quality of life for patients worldwide.

PLRC's central offering is the PLRC Registry, a patient-designed digital platform hosted via mydatahelps.org that connects individuals with Long COVID and associated conditions to clinical trials and research studies. The organization surrounds this registry with a portfolio of complementary programs: the Hypothesis Journal (a peer publication of patient-generated research hypotheses, with Issue 1 released Spring 2023 and Issue 2 released Summer 2024), Patient Engagement Scorecards (a downloadable PDF assessment tool for measuring patient engagement in research), a Patient-Led Research Fund that provides grants to patient-led initiatives, a Clinical Trials information hub, and PLRC Advisory Services for researchers, clinicians, and organizations. Distribution occurs primarily through its website (patientresearchcovid19.com), email newsletter, earned media, and advocacy outreach.

As a non-profit, PLRC does not operate a traditional commercial revenue model. The organization solicits donations (a "Donate" call-to-action is prominent on the site), operates the Patient-Led Research Fund, and offers paid Advisory Services to researchers, clinicians, and organizations. The technology stack centers on a self-serve web platform with the registry powered through a third-party patient-data tool (mydatahelps.org), rather than proprietary enterprise software. Customer segments include patients with Long COVID (primary), Long COVID researchers, and clinicians, with the global audience reached through digital content and advocacy channels.

Short descriptiontext

Patient-Led Research Collaborative is a non-profit founded in 2020 that operates the PLRC Registry and related programs to connect Long COVID patients with clinical trials, publish patient-generated research hypotheses, and advocate for improved patient care policies globally.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
Markets served

Serves global market

Keyword5 values
patient registry platform, long COVID research, clinical trial matching, patient engagement tools, infection-associated research
Industry1 code
1Electronic Data Capture (EDC) Platforms
CodeHLACAOAAPrimaryYes
NAICS code1 code
  • Software Publishers513210
SIC code2 codes
  • Services-Prepackaged Software7372
  • Services-Computer Programming, Data Processing, Etc.7370
Product category
Patient Advocacy and Research Services
Social media profiles1 record
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Personnel, Technology or R&D, Operations, Marketing or Sales
GTM typeB2B and B2C
B2B and B2C
Offering typeServices
Services
Core offering1 text field

PLRC is a non-profit patient-led research collaborative focused on Long COVID and infection-associated chronic conditions. It provides the PLRC Registry platform where patients share health data and surface research hypotheses, advisory services for researchers and clinicians, and the Patient-Led Research Fund to support related scientific studies. The organization also publishes resources such as the Hypothesis Journal and Patient Engagement Scorecards.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Patient-Led Research Collaborative (PLRC) is a patient-centered research organization offering a portfolio of interconnected programs. The core offering is the PLRC Registry—a patient-designed platform connecting individuals with clinical trials and research studies. Supporting programs include the Hypothesis Journal (a patient-generated research publication), Patient Engagement Scorecards (assessment tools), the Patient-Led Research Fund (grant program), Clinical Trials information access, and Advisory Services. The organization focuses on improving research into Long COVID and infection-associated chronic conditions through patient-centered, equitable approaches.

Product and service3 records
1PLRC Registry
CategoryPatient registry platform
Description

Proprietary digital registry platform that allows patients with Long COVID and infection-associated chronic conditions to share health data, contribute symptom and experience information, surface research hypotheses, and connect with relevant clinical trials and research opportunities. Targeted at patients living with these conditions.

2PLRC Advisory Services
CategoryAdvisory and consulting services
Description

Advisory offering for researchers, clinicians, and organizations working on Long COVID and infection-associated chronic illnesses, providing guidance on patient-engaged research design, methodology, and patient recruitment.

3Patient-Led Research Fund
CategoryResearch grant program
Description

Grant program that provides funding to scientific studies focused on Long COVID and infection-associated chronic conditions, channeling resources to research aligned with the patient-led agenda.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers8 records
TypeDirect peer
Description

Patient-led online platform where members share health data and connect with research studies across chronic conditions. Directly comparable to PLRC Registry's model of connecting patients with clinical trials and generating patient-centered research insights.

TypeEmerging player
Description

Nonprofit focused on patient advocacy, genetic and rare disease research infrastructure, and registry development. Comparable to PLRC as a patient-driven research organization building engagement tools and resources.

TypeBroad incumbent
Description

Established patient-driven foundation that funds a disease-specific research pipeline and registry. Comparable to PLRC as the canonical patient-led research funding model, though operating at vastly greater scale with a different disease focus.

TypeBroad incumbent
Description

NIH-led million-person precision medicine registry that recruits diverse participants and shares data with researchers. Comparable as a large-scale patient registry feeding clinical research, though federally funded and condition-agnostic rather than patient-led and disease-specific.

TypeDirect peer
Description

Clinical trial matching platform that uses structured data to connect patients with relevant trials. Comparable to PLRC Registry in the trial-recruitment use case, though Antidote operates commercially across many conditions.

TypeDirect peer
Description

Coalition advancing Long COVID research, patient care, and policy. Directly comparable to PLRC's advocacy-driven approach and Long COVID focus, though operating as a coalition rather than a patient-led research collaborative.

7CURE ID
TypeEmerging player
Description

NIH/NCATS-led app and platform for crowdsourcing clinician-reported treatment outcomes and connecting patients to clinical trials. Comparable as a federally backed patient-to-research pipeline overlapping PLRC Registry's core function.

8Body Politic
TypeDirect peer
Description

Foundational Long COVID patient-led support and advocacy community that helped catalyze the patient-driven Long COVID research movement. Directly comparable as a patient-led Long COVID organization focused on advocacy and research coordination.

Market position
Strengths3 records

Each record includes

Headline, Details, Source

Weaknesses3 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks4 records

Each record includes

Headline, Details, Source

Key highlights4 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature1 record

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Patient-Led Research Collaborative

Patient Advocacy and Research Servicespatientledresearch.com

Patient-Led Research Collaborative is a non-profit founded in 2020 that operates the PLRC Registry and related programs to connect Long COVID patients with clinical trials, publish patient-generated research hypotheses, and advocate for improved patient care policies globally.

What Patient-Led Research Collaborative does

The Patient-Led Research Collaborative (PLRC) is an international non-profit research organization founded in 2020 that focuses on improving research into Long COVID and infection-associated chronic conditions. It is staffed by approximately 10 individuals who themselves live with these conditions and come from diverse professional backgrounds. The organization's stated mission is to advance the breadth, depth, and speed of global research and to advocate for policies that improve quality of life for patients worldwide.

PLRC's central offering is the PLRC Registry, a patient-designed digital platform hosted via mydatahelps.org that connects individuals with Long COVID and associated conditions to clinical trials and research studies. The organization surrounds this registry with a portfolio of complementary programs: the Hypothesis Journal (a peer publication of patient-generated research hypotheses, with Issue 1 released Spring 2023 and Issue 2 released Summer 2024), Patient Engagement Scorecards (a downloadable PDF assessment tool for measuring patient engagement in research), a Patient-Led Research Fund that provides grants to patient-led initiatives, a Clinical Trials information hub, and PLRC Advisory Services for researchers, clinicians, and organizations. Distribution occurs primarily through its website (patientresearchcovid19.com), email newsletter, earned media, and advocacy outreach.

As a non-profit, PLRC does not operate a traditional commercial revenue model. The organization solicits donations (a "Donate" call-to-action is prominent on the site), operates the Patient-Led Research Fund, and offers paid Advisory Services to researchers, clinicians, and organizations. The technology stack centers on a self-serve web platform with the registry powered through a third-party patient-data tool (mydatahelps.org), rather than proprietary enterprise software. Customer segments include patients with Long COVID (primary), Long COVID researchers, and clinicians, with the global audience reached through digital content and advocacy channels.

Patient-Led Research Collaborative firmographics

Firmographics
Name
Patient-Led Research Collaborative
Legal name
Patient Led Research Collaborative
Website
https://patientledresearch.com
Company type
Private
Operating status
Operating
Headcount range
1–10 employees
Short description
Patient-Led Research Collaborative is a non-profit founded in 2020 that operates the PLRC Registry and related programs to connect Long COVID patients with clinical trials, publish patient-generated research hypotheses, and advocate for improved patient care policies globally.
Ownership category
akta.pro rank

Patient-Led Research Collaborative industry classification

Industry
Product category
Patient Advocacy and Research Services
NAICS
Software Publishers (513210)
SIC
Services-Prepackaged Software (7372), Services-Computer Programming, Data Processing, Etc. (7370)
akta.pro primary industry
Electronic Data Capture (EDC) Platforms (HLACAOAA)

Keywords

  • Patient registry platform
  • Long COVID research
  • Clinical trial matching
  • Patient engagement tools
  • Infection-associated research

Patient-Led Research Collaborative business model

Business model
GTM type
B2B and B2C
Offering type
Services
Cost components
Personnel, Technology or R&D, Operations, Marketing or Sales

Distribution channels1 record

Marketing channels4 records

Patient-Led Research Collaborative product offering

Product offering

Core offering

PLRC is a non-profit patient-led research collaborative focused on Long COVID and infection-associated chronic conditions. It provides the PLRC Registry platform where patients share health data and surface research hypotheses, advisory services for researchers and clinicians, and the Patient-Led Research Fund to support related scientific studies. The organization also publishes resources such as the Hypothesis Journal and Patient Engagement Scorecards.

Product overview

Patient-Led Research Collaborative (PLRC) is a patient-centered research organization offering a portfolio of interconnected programs. The core offering is the PLRC Registry—a patient-designed platform connecting individuals with clinical trials and research studies. Supporting programs include the Hypothesis Journal (a patient-generated research publication), Patient Engagement Scorecards (assessment tools), the Patient-Led Research Fund (grant program), Clinical Trials information access, and Advisory Services. The organization focuses on improving research into Long COVID and infection-associated chronic conditions through patient-centered, equitable approaches.

Differentiator

Problem solved

Functional benefit

Products and services

  • PLRC Registry Proprietary digital registry platform that allows patients with Long COVID and infection-associated chronic conditions to share health data, contribute symptom and experience information, surface research hypotheses, and connect with relevant clinical trials and research opportunities. Targeted at patients living with these conditions.
  • PLRC Advisory Services Advisory offering for researchers, clinicians, and organizations working on Long COVID and infection-associated chronic illnesses, providing guidance on patient-engaged research design, methodology, and patient recruitment.
  • Patient-Led Research Fund Grant program that provides funding to scientific studies focused on Long COVID and infection-associated chronic conditions, channeling resources to research aligned with the patient-led agenda.

Companies that use Patient-Led Research Collaborative

Customer profile

Segments3 records

Ideal customer profiles2 records

Patient-Led Research Collaborative technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature1 record

Patient-Led Research Collaborative partnerships and signals

Strategic signal

Scale indicators1 record

Recent moves5 records

Expansion highlights4 records

Patient-Led Research Collaborative competitors and assessment

Company assessment

Direct peers

  • PatientsLikeMe: Patient-led online platform where members share health data and connect with research studies across chronic conditions. Directly comparable to PLRC Registry's model of connecting patients with clinical trials and generating patient-centered research insights.
  • Antidote: Clinical trial matching platform that uses structured data to connect patients with relevant trials. Comparable to PLRC Registry in the trial-recruitment use case, though Antidote operates commercially across many conditions.
  • Long COVID Alliance: Coalition advancing Long COVID research, patient care, and policy. Directly comparable to PLRC's advocacy-driven approach and Long COVID focus, though operating as a coalition rather than a patient-led research collaborative.
  • Body Politic: Foundational Long COVID patient-led support and advocacy community that helped catalyze the patient-driven Long COVID research movement. Directly comparable as a patient-led Long COVID organization focused on advocacy and research coordination.

Emerging players

  • Genetic Alliance: Nonprofit focused on patient advocacy, genetic and rare disease research infrastructure, and registry development. Comparable to PLRC as a patient-driven research organization building engagement tools and resources.
  • CURE ID: NIH/NCATS-led app and platform for crowdsourcing clinician-reported treatment outcomes and connecting patients to clinical trials. Comparable as a federally backed patient-to-research pipeline overlapping PLRC Registry's core function.

Broad incumbents

  • Cystic Fibrosis Foundation: Established patient-driven foundation that funds a disease-specific research pipeline and registry. Comparable to PLRC as the canonical patient-led research funding model, though operating at vastly greater scale with a different disease focus.
  • All of Us Research Program: NIH-led million-person precision medicine registry that recruits diverse participants and shares data with researchers. Comparable as a large-scale patient registry feeding clinical research, though federally funded and condition-agnostic rather than patient-led and disease-specific.

Market position

Strengths3 records

Weaknesses3 records

Competitive moat4 records

Key risks4 records

Key highlights4 records

Customer concentration

Patient-Led Research Collaborative social profiles

Digital presence

Patient-Led Research Collaborative financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Patient-Led Research Collaborative leadership team

Management profile

Number of profiles

Patient-Led Research Collaborative funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Patient-Led Research Collaborative M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Patient-Led Research Collaborative

What does Patient-Led Research Collaborative do?

PLRC is a non-profit patient-led research collaborative focused on Long COVID and infection-associated chronic conditions. It provides the PLRC Registry platform where patients share health data and surface research hypotheses, advisory services for researchers and clinicians, and the Patient-Led Research Fund to support related scientific studies. The organization also publishes resources such as the Hypothesis Journal and Patient Engagement Scorecards.

Is Patient-Led Research Collaborative a public or private company?

Patient-Led Research Collaborative is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was Patient-Led Research Collaborative founded?

Patient-Led Research Collaborative was founded in -1. It employs 1 to 10 people.

Who are Patient-Led Research Collaborative's main competitors?

Direct peers on record are PatientsLikeMe, Antidote, Long COVID Alliance and Body Politic. Emerging players are Genetic Alliance and CURE ID. Broad incumbents are Cystic Fibrosis Foundation and All of Us Research Program.

Does Patient-Led Research Collaborative have an API?

No public API is recorded for Patient-Led Research Collaborative.

What industry is Patient-Led Research Collaborative in?

Patient-Led Research Collaborative's product category is Patient Advocacy and Research Services. Its primary akta.pro industry code is HLACAOAA, Electronic Data Capture (EDC) Platforms. Its NAICS code is 513210 and its SIC code is 7372.

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