Pipeline Alert: Gameto $44M Series C

Gameto raises $44M Series C. Target eClinical trial software & CDMO services. Email CEO Dina Radenkovic. 💰

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🚀 Battle Card: Gameto

Quick trigger:
 
👤 Decision Maker in the News
 
💡 Why It Matters
  • The $44M boost fuels acceleration of Phase 3 cell-engineered ovarian-aging therapies, highlighting investment in trial software and manufacturing capacity. This Gameto sales trigger signals priority spend on eClinical and CDMO partners. → Source
 
🎯 Core Pain Point
  • Scaling GMP-compliant cell production for Phase 3 ovarian cell therapies
  • Managing complex trial data capture and regulatory compliance
 
💰 What to Pitch
  • Primary: eClinical Trial Management Software → streamline Phase 3 data capture & analysis
  • Expansion: GMP Cell Therapy Manufacturing Service → scale granulosa & oocyte precursor production
 
🗺️ Quick Context
  • HQ: New York, NY
  • Employees: ≈ 75
  • Rev: ≈ $0 (pre-revenue)
 

🤼 Competitive Intel

Which other vendors you’ll probably face to win Gameto’s business.
 
  • MedidataeClinical Trial Software
    • Unique edge: Industry-leading EDC & RTSM platform
    • Evaluated by VP Clinical for data reliability
  • Veeva SystemseClinical Trial Software
    • Unique edge: Unified CRM, regulatory & trial operations
    • Evaluated by CMO for integrated compliance
  • Oracle Health ScienceseClinical Trial Software
    • Unique edge: Scalable global trial infrastructure
    • Evaluated by Head of R&D for analytics depth
  • LonzaCDMO / Cell Therapy Manufacturing
    • Unique edge: Full-spectrum process development & scale-up
    • Evaluated by VP Manufacturing for scale expertise
  • CatalentCDMO / Cell Therapy Manufacturing
    • Unique edge: Flexible facility networks & fill-finish
    • Evaluated by QA & VP Clinical for CMC support
  • WuXi AppTecCDMO / Cell Therapy Manufacturing
    • Unique edge: End-to-end testing & production services
    • Evaluated by QA for quality assurance
 

✅ Do-Now Checklist

Reference the Gameto sales trigger in your first outreach
Schedule follow-ups in CRM (Day 3 & Day 10)
 

Next Step

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🧠 Copy My Prompt for Personalized Cold Outreach

────────────────────────────
✏️ YOUR COMPANY
────────────────────────────
OUR_COMPANY   = ❑<your company>❑
OFFER_BRIEF   = ❑Streamlined Phase 3 eClinical trial data capture & analysis❑
PROOF_METRIC  = ❑≈ TBD❑
CTA_STYLE     = ❑quick_call❑
TONE          = ❑punchy❑

────────────────────────────
📌 TARGET COMPANY
────────────────────────────
NAME        = Dina
COMPANY     = Gameto
DEPT        = R&D
SIZE        = 75
BOTTLENECK  = scaling GMP-compliant cell production for Phase 3 ovarian cell therapies
EVENT       = Closes $44M Series C Round
DETAIL      = Closes $44M Series C Round
PAIN        = managing complex trial data capture and regulatory compliance
SRC         = https://vcnewsdaily.com/gameto/venture-capital-funding/ndxrvhgjbb
SIM_CO      = ≈ TBD
WIN_METRIC  = ≈ TBD
NEXT_SIZE   = 150
EMP_EST     = ≈ 75
REV_EST     = ≈ $0M

────────────────────────
TASK FOR CHATGPT
────────────────────────
Role: “NewsletterForLeads SDR-Assist”.

Validate any ≈ guesses via SRC.

EMAIL  (keep breaks):
Subject: 75-person R&D

Dina—noticed your R&D team is ≈ 75.

That’s when scaling GMP-compliant cell production for Phase 3 ovarian cell therapies slows growth.

We helped ≈ TBD fix this with Streamlined Phase 3 eClinical trial data capture & analysis.

Result: ≈ TBD.  
Quick call?

PS—next bottleneck hits ≈ 150.

DM ≤45 words, TONE:
Saw your post about Closes $44M Series C Round — managing complex trial data capture and regulatory compliance.  
Streamlined Phase 3 eClinical trial data capture & analysis. ≈ TBD.  
Quick chat?

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