The Collaborative invites applications for innovative research strategies that directly address pediatric, adolescent or young adult cancers through a novel idea built around one of the Focus Areas and the Priority Area outlined in Section II. These grants are designed to provide seed funding for a new idea that may not have preliminary data but for which a strong case can be made for the potential impact for children, adolescents and young adults battling cancer.
Focus and Priority Areas
The application must address one Focus Area and the Priority Area related to cancer in children (0-14), adolescents (15-19) and/or young adults (20-24):
Focus Areas:
• Leverage the use of artificial intelligence to advance the diagnosis, treatment or understanding of cancer in children, adolescents and young adults with a demonstrated potential for clinical translation.
• Advance efficiency, coordination and overall quality of cancer care to improve outcomes for children, adolescents and young adults as well as their families. Priority will be given to research that:
• Incorporates patient- and family-centered approaches to improve the experience and delivery of care across settings (inpatient, outpatient and virtual);
• Leverages health information technology, artificial intelligence or decision-support tools to enhance care coordination, resource utilization or treatment planning;
• Aims to improve clinical trials by addressing challenges unique to pediatric populations to increase accessibility, speed and scientific impact; or
• Aims to improve pediatric clinical trials by streamlining regulatory approvals.
Priority Area:
• A novel idea for innovative research that could lead to advanced studies, better delivery of treatment or clinical translation.
The following will not be reviewed:
• Grants that have no direct relevance to pediatric cancer nor fall within the scope of A Collaborative Pediatric Cancer Research Awards Program.
• Proposals for infrastructure programs.
• Incomplete applications and/or applications received after the deadline.
Award Information
Outside the Box Grants award up to $50,000 for one year of support. One-year grants will receive two installments, one every six months.
Rally is highly pediatric-specific.
Strong proposals:
focus on children or AYA oncology biology
justify why the target cannot be studied solely in adults
acknowledge unique pediatric tumor biology
Vague “oncology in general” = low competitiveness.
Funding tends to favor work that could:
guide therapy selection,
improve survival curves,
reduce treatment toxicity,
enable clinical trial readiness.
Purely descriptive molecular biology is weaker.
Higher award frequency in:
Ewing sarcoma
Neuroblastoma
Medulloblastoma
Osteosarcoma
Rhabdomyosarcoma
Diffuse intrinsic pontine glioma (DIPG)/DMG
Proposals that address rarity-associated resource scarcity score well.
Consistently favored:
next-gen immunotherapies (CAR, BiTEs, NK)
genomics-driven vulnerability mapping
tumor microenvironment targeting
ex vivo drug screening platforms
resistance mechanism deconvolution
Incremental extensions do poorly.
Even pilot-stage grants reward:
feasibility demonstration
target validation
early pharmacodynamic rationale
drug sensitivity assays
Preliminary animal or organoid data strengthen scoring.
Rally grants are modest (~$50–$100k/yr). Past reviewers penalize:
multi-omics pipelines requiring major infrastructure
assay development from scratch
Scope realism is a key success factor.
Successful applicants clearly articulate:
survival gains,
toxicity mitigation,
reduced late effects,
QoL improvements.
Reviewers are advocacy- and family-informed.
Rally stands out for:
cultivating pediatric oncology independence
training pipeline reinforcement
Clear mentorship plans matter.
Helpful signals:
COG participation
access to pediatric biospecimens
multi-institutional validation
Not required, but historically common.
Look for commitments:
protected time
reagent availability
core facility access
biostatistics support
Generic letters are penalized.
Common among funded investigators:
PDX or PDO models
single-cell profiling
immune landscape characterization
drug repurposing screens
kinase dependency mapping
Techniques are hypothesis-driven, not fishing expeditions.
Rally responds to:
relapsed/refractory disease
treatment-resistant clones
metastasis biology
long-term toxicities in survivors
Therapy de-escalation is increasingly favored.
Recurring summary phrases include:
“Compelling translational rationale.”
“Appropriately powered pilot.”
“Promising investigator trajectory.”
“Access to relevant pediatric samples.”
Predictors of rejection:
✘ extrapolated from adult oncology without pediatric justification
✘ unfocused aims (more than 2–3)
✘ lack of preliminary efficacy signal
✘ no path to clinical readiness
✘ unrealistic timelines
Successful applications demonstrate:
feasible effect sizes,
clear endpoints,
biomarker stratification plans.
Hand-wavy statistical sections get flagged.
Rally reviewers favor:
prognostic stratification tools,
actionable therapeutic biomarkers,
minimal residual disease (MRD).
Merely associative signatures are weaker.
Patterns visible across years:
Patient narrative framing matters.
Justifying sample scarcity matters.
Clear line of sight to a future clinical trial matters.
Most successful proposals follow:
Aim 1: Define/validate a targetable vulnerability in a pediatric tumor.
Aim 2: Test therapeutic perturbation in physiologically relevant models.
Aim 3 (optional): Biomarker strategy for clinical translation.
Two aims for early-career investigators often outperform three.
High-yield budget elements:
animal models
sequencing validation
reagents (antibodies, inhibitors)
core facility charges
Low-yield:
personnel bloat
large capital purchase requests
Rally values:
hope messaging
urgency
community involvement in research direction
Aligning your narrative with this ethos adds intangible advantage.
A competitive Rally proposal is:
✅ pediatric-specific
✅ clinically translatable
✅ supported by preliminary data
✅ small-grant feasible
✅ focused on relapse/resistance/toxicity
✅ linked to a future trial or IND trajectory
Weak proposals are:
✘ mechanistically interesting but clinically distant
✘ adult-only tumor biology extended to children without justification
✘ under-mentored
✘ over-ambitious
• Applicants conducting pediatric cancer research as a clinical fellow in pediatric hematology/oncology and/or postdoctoral research fellow. Applicants must hold at least an M.D., D.O., Pharm.D. or Ph.D. degree and be conducting research after the first year of their fellowship.
• Applicants with all academic ranks, Instructor to Professor, and research scientists holding at least an M.D., D.O., Pharm.D. and/or Ph.D. degree may apply.
On the application Face Page, the applicant will identify themselves as a Young Investigator or an Independent Investigator. Rally defines young investigators as principal investigators no more than five years post fellowship and independent investigators as principal investigators more than five years post fellowship.
• Applicants do not need to be U.S. citizens or located at a U.S. institution.
• The applicant’s institution may be a hospital, university or private lab.
Sponsor Institute/Organizations: Rally Foundation for Childhood Cancer Research
Sponsor Type: Corporate/Non-Profit
Address: 5775 Glenridge Drive Building B, Suite 370 Atlanta, GA 30328
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Jan 06, 2026
Jan 06, 2026
$50,000
Affiliation: Rally Foundation for Childhood Cancer Research
Address: 5775 Glenridge Drive Building B, Suite 370 Atlanta, GA 30328
Website URL: file:///C:/Users/Administrator/Downloads/PRDESC5221.pdf
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