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Funding Opportunity




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The Francis S. Collins Scholars Program in Neurofibromatosis Clinical and Translational Research

Neurofibromatosis Therapeutic Acceleration Program

Program overview

The Francis S. Collins Scholars Program is for talented post-doctoral researchers or early-career faculty members looking to make a significant impact in clinical and translational research for NF1.

Named for the pioneering scientist who led a team that discovered the NF1 gene in 1990, The Francis S. Collins Scholars Program accepts applications from candidates who are committed to advancing the frontiers of NF1 research and clinical care. This highly competitive program, which was launched in 2014, has inducted close to 20 clinician scientists who now hold positions of leadership in the field. It provides formal training in clinical and translational science, mentorship from leaders in NF1 and related fields, and clinical training for the care of patients with NF1.

As a Francis S. Collins Scholar, you will receive up to 100% salary support for NF1-associated clinical, research, educational and mentorship activities.

This is a career-changing opportunity to join a community of scientists committed to making a lasting impact in NF1 research and clinical care.

Funding, mentoring and resources

  • Full salary for 3 years
  • Training in the care of NF1 patients
  • Tuition support and formal training in clinical translational science
  • Participation in collaborative translational research programs with government, academic and industry partners
  • Funding for research costs
  • Travel costs for scientific meetings
  • High-level mentoring support from top scientists

AI Based Application Success Predictor

1. Absolute, Explicit Focus on NF1 Therapeutic Development

NTAP is laser-focused on accelerating treatments for:

Plexiform neurofibromas (PN)

Cutaneous neurofibromas (cNF)

NF1 tumor biology and therapeutic vulnerabilities

Projects must show a direct path toward therapy development.

Commonly funded areas:

Drug discovery or drug repurposing

Biomarker discovery for therapeutic monitoring

Preclinical models testing treatment response

Molecular pathways that drive PN or cNF

Therapeutic target validation

Translational studies linking patient samples to therapy development

Predictor: If a proposal is not directly linked to creating or advancing a therapy, it rarely succeeds.

2. Fit to NTAP’s Strategic Priorities

NTAP regularly communicates strategic focus areas such as:

Model systems enabling therapy development (organoids, PDX, genetic models)

Response biomarkers for trials

Drug screening platforms

Cutaneous neurofibroma treatment pathways

Combination therapy rationales

Mechanisms of resistance to MEK inhibitors (e.g., selumetinib)

Clinical trial-enabling studies

Predictor: Align your proposal with a clearly identified NTAP strategic gap, not a generic NF1 study.

3. Strong Preliminary Data Demonstrating Feasibility

NTAP expects evidence that:

The model or system works

The therapeutic target is promising

Pilot efficacy data supports further testing

Human tissue or cell access is secured

Necessary collaborations are in place

Predictor: Robust pilot data is one of the strongest indicators of competitiveness.

4. Emphasis on Translational or Preclinical Impact

NTAP is not a basic research foundation.

Successful applications show:

A defined translational endpoint (e.g., drug lead, biomarker, trial-ready intervention)

Work that can move quickly into IND-enabling or clinical feasibility steps

A timeline that fits within 1–2 years for concrete outcomes

Predictor: Translational relevance is essential.

5. Use of NF1-Relevant Human Samples or Valid Models

Strong proposals leverage:

NF1 patient-derived cells

cNF or PN tissue samples

NF1 organoids, spheroids, or engineered systems

NF1 mouse models (e.g., Nf1 floxed lines, Dhh-Cre, Prss56 models)

Data from natural history studies or clinical cohorts

Predictor: Use of disease-relevant, validated NF1 models significantly boosts competitiveness.

6. Clear, Focused Specific Aims with Measurable Milestones

NTAP-funded projects typically include:

2–3 tightly scoped aims

Milestone-based design (go/no-go gates)

Well-defined preclinical endpoints

Short timelines with feasible execution

Risk mitigation strategies

Predictor: Concrete deliverables and milestones are highly valued.

7. Strong Collaboration and Multi-Disciplinary Expertise

NTAP is deeply collaborative and encourages:

Multi-PI or multi-institution teams

Integration of molecular biology + pharmacology + clinical insights

Partnerships with NF clinical trial consortia

Shared data and resource plans

Predictor: Proposals with cross-disciplinary and multi-site teams score higher.

8. Strong Justification Based on Patient Need

Funded projects often articulate:

A critical unmet need (e.g., few options for cNF treatment)

How the project accelerates therapy timelines

How outcomes will affect NF1 patient care

Pathways for future clinical translation

Predictor: Patient-centered framing improves impact score.

9. Clear Institutional Support & Resources

Successful applications demonstrate:

Access to NF1 clinical cohorts

Access to patient samples

Bioinformatics, pharmacology, or imaging cores

Departmental support, protected time, and infrastructure

Predictor: Strong environment increases reviewer confidence.

10. Highly Polished, Reviewer-Friendly Writing

Top-scoring NTAP proposals:

Are very clear and concise

Provide strong visual preliminary data

Explain rationale in NF1 context, not general cancer biology

Make translational impact explicit

Clearly outline expected therapeutic acceleration steps

Predictor: Clear storytelling elevates scoring and enthusiasm.

🏆 Summary Table — NTAP Success Predictors

PredictorWhy It Matters
Direct NF1 therapeutic relevanceCore mission requirement
Alignment with NTAP prioritiesEnsures reviewer excitement
Strong preliminary dataDemonstrates feasibility
Translational/preclinical focusNTAP is therapy-driven
NF1-relevant modelsEnsures human relevance
Clear, milestone-driven aimsFits NTAP project structure
CollaborationsEnhances impact and feasibility
Patient-centered justificationAligns with mission impact
Strong environmentSupports execution
Clear writingImproves reviewer enthusiasm

  • Must hold a health professional degree that permits patient care and be committed to engaging in clinical care.
  • Commit at least 75% of professional time to the program for a minimum of two years and a maximum of three years.
  • Be in the last year of post-doctoral training or be a junior faculty member within seven years of the first faculty appointment.
  • Have a commitment to patient-focused research in the field of NF1.
  • Demonstrate prior research commitment and accomplishments.
  • Have a team of up to four people that includes research, clinical, and career mentors who are committed to the candidate’s training, expertise in the proposed research skill set, and in the clinical management of NF1.
  • Agree to meet all of the requirements of the Francis S. Collins Scholars Program in Neurofibromatosis Clinical and Translational Research, including participation in required Scholars meetings and activities.

Sponsor Institute/Organizations: Neurofibromatosis Therapeutic Acceleration Program

Sponsor Type: Corporate/Non-Profit

Address: 600 North Wolfe Street, Meyer 8-149, Baltimore, MD 21287.

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Grant

Letter Of Intent Deadline:

Dec 08, 2025

Final Deadline:

Dec 08, 2025

Funding Amount:

$25,000

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