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Development of Continuous CPeptide Monitoring Technologies

Breakthrough T1D

• Breakthrough T1D invites applications to develop continuous C-peptide monitoring (CCPM) technologies.

• Applications focused on early-stage development of sensor technologies, preclinical/feasibility studies and early-stage clinical evaluation of CCPM technologies will be considered.

• Applications may request up to $900,000 in total funding over a maximum period of three years. Applications of increased scope (time and/or budget) will be considered where there is a strong justification. Interested applicants should discuss with the Breakthrough T1D scientific contact, aghavami@breakthrought1d.org

Funding Opportunity Description

Breakthrough T1D is the world’s leading non-profit organization dedicated to curing and improving the lives of people with type 1 diabetes (T1D) by accelerating breakthroughs for T1D. T1D is a chronic autoimmune condition characterized by the destruction of insulin-producing beta cells in the pancreas, resulting in hyperglycemia and dependence on exogenous insulin. C-peptide, a byproduct of endogenous insulin production, is widely recognized as a biomarker of beta cell function. However, current monitoring methods—such as stimulated tests (e.g., glucagon stimulation) and point-of-care (POC) assays that assess basal levels without stimulation—are invasive, time-consuming, and limited to single time-point measurements in clinical settings1. These approaches are poorly suited to capturing the dynamic nature of C-peptide secretion, and they offer limited utility for real-world, longitudinal monitoring. In particular, they are not well suited for detecting early beta cell changes following interventions such as disease modifying therapies (immunotherapies or beta cell preservation agents) or beta cell replacement. For example, they may fail to reliably detect early engraftment or subtle graft dysfunction following cell implantation. To address these limitations, Breakthrough T1D invites applications to develop continuous C-peptide monitoring (CCPM) technologies. These efforts aim to expand capabilities in research and care by enabling more detailed, real-time, and user-friendly assessments of beta cell function over time. CCPM has the potential to improve our understanding of T1D progression and to support the development and evaluation of disease-modifying and cell-based therapies.

Funding Mechanisms

In response to this announcement, applications may request up to a total of $900,000 USD for up to three years.

• The level of funding will vary depending on the scope and overall objectives of the proposal. Breakthrough T1D may consider applications with increased scope (time, budget) where there is a strong justification, and applicants interested in such should discuss with the Breakthrough T1D scientific contact below.

• Note that the above budget figure is a maximum, and Breakthrough T1D will also consider projects with substantially smaller budgets. In all cases, the level of requested funding should be commensurate with the studies proposed and non-Breakthrough T1D resources (funds, personnel, other) available to successfully complete the project. Appropriateness of budget in relation to scope will be considered as part of the review criteria.

AI Based Application Success Predictor

While competitive specifics can vary by mechanism, proposals that win funding consistently share these strengths:

✅ 1) Alignment with Strategic Priorities

Your project must clearly connect to Breakthrough T1D’s mission — curing T1D and improving lives — or to a specific funding opportunity’s focus area (e.g., tolerance in islet replacement, monitoring technologies, clinical relevance). Breakthrough T1D+1

Tip: Explicitly justify which strategic goal(s) your work addresses in both the LOI and full proposal.

✅ 2) Clear, Impactful Scientific Rationale

Successful applications present:

A strong, evidence-based rationale for why the research matters,

Well-defined hypotheses or objectives,

Direct significance to T1D biology, clinical outcomes, or technology gaps.

Breakthrough T1D prioritizes work likely to accelerate translation toward therapy development. Breakthrough T1D

✅ 3) Feasible Study Design With Realistic Milestones

Proposals that are clearly executable in the funding timeframe—with thoughtful experimental design, milestones, and contingency planning — score higher during review.

Include:

Detailed methods

Milestones tied to measurable outcomes

A realistic timeline

✅ 4) Strong Team and Institutional Capacity

Breakthrough T1D often reviews:

Investigator track record,

Institutional resources and support,

Collaborations that enhance feasibility and reach.

Demonstrate that your team has the expertise and facilities to deliver on the proposal. Breakthrough T1D

✅ 5) Meaningful Translation and Clinical Relevance

Even for basic science, reviewers value work that lays clear groundwork for translation — for example:

Biomarkers predictive of disease progression,

Platforms or tools that shorten clinical testing,

Approaches ready for next-step clinical studies.

Make translational potential explicit in aims and impact statements.

✅ 6) Balanced Budget Justification

Grants like Innovative Awards (~$200 k/1 yr) and SRAs (up to ~$900 k/3 yrs) require budgets that are justified and aligned with deliverables. Overly optimistic or under-budgeted proposals are less competitive. Breakthrough T1D+1

✅ 7) Engagement With Stakeholders & Ethics

Where relevant (especially clinical research or novel technologies), strong ethics planning and stakeholder engagement (including patient populations) boost confidence in feasibility and impact.

✅ 8) Clear Communication & Strategic Positioning

Given the volume of submissions and variety of expert reviewers, clarity of narrative with defined aims and outcomes is crucial. Strong summary sections (abstract and lay summary) effectively ‘sell’ the project.

🧠 Grant Review Structure

Breakthrough T1D typically uses a two-stage review:

LOI screening – checks alignment and concept strength.

Full proposal review – detailed scientific and feasibility assessment. Breakthrough T1D

Some calls (e.g., Innovative Awards) may go directly to full proposal.

📌 Typical Funding Amounts & Duration

Mechanism	Award Size	Duration
Innovative Awards	Up to ~$200,000	1 year Breakthrough T1D
Strategic Research Agreements	Up to ~$900,000	Up to 3 years Breakthrough T1D UK
Mechanism-specific Calls	Varies by topic	Varies by program Breakthrough T1D

🧠 Final Summary: Breakthrough T1D Success Predictors

Top predictors of funding competitiveness:

🔹 Strong fit with Breakthrough T1D’s mission and specific call focus. Breakthrough T1D

🔹 Science with clear impact on cure pathways or life improvement. Breakthrough T1D

🔹 Feasible design with milestones and measurable outcomes.

🔹 Experienced research team and institutional support.

🔹 Translational vision connecting bench progress to real-world outcomes.

🔹 Well-justified, realistic budget.

🔹 Communicative clarity and strategic narrative.

Specialties

Clinical Trials

Eligibility Requirements

• Applications may be submitted by domestic and foreign non-profit organizations, public and private, such as universities, colleges, hospitals, laboratories, units of state and local governments, and eligible agencies of the federal government. Applicants must hold an M.D., D.O., D.M.D., D.V.M., Ph.D., or equivalent and have a faculty position or equivalent at a college, university, medical school, or other research facility.

• To assure continued excellence and diversity among applicants and awardees, Breakthrough T1D welcomes proposals from all qualified individuals and encourages proposals from a broad cross section of researchers and scientists

Sponsor Details

Sponsor Institute/Organizations: Breakthrough T1D

Sponsor Type: Corporate/Non-Profit

Address: 200 Vesey Street, 28th Floor, New York, NY 10281

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