CRISPR Therapeutics

Company CRSP

Last mentioned: Mar 11, 2026

Timeline

  1. Offering Upsized

    The company prices an upsized $550M offering due to strong institutional interest.

  2. ARK Invest Trade

    Cathie Wood's ARK Invest buys the dip, increasing its position in CRSP shares.

  3. Debt Offering Announced

    CRISPR Therapeutics announces a $350M convertible senior notes offering, causing a stock price dip.

  4. Cure Announcement

    Medical officials formally announce the patient is cured, marking a global first for gene editing technology.

  5. Six-Month Follow-up

    Clinical evaluations confirm significant biological markers of recovery and the absence of off-target effects.

  6. Therapy Administration

    A one-time gene editing intervention is administered at a specialized pediatric facility in British Columbia.

  7. Trial Enrollment

    The B.C. teen is enrolled in a world-first experimental gene editing clinical trial for a rare genetic disorder.

Stories mentioning CRISPR Therapeutics 3

markets Neutral

Cathie Wood Capitalizes on CRISPR Therapeutics Dip Amid $550M Debt Offering

ARK Invest founder Cathie Wood has increased her stake in CRISPR Therapeutics following a stock price decline triggered by a significant convertible debt offering. The move underscores Wood's long-term conviction in the gene-editing sector despite short-term market volatility and capital-raising pressures.

2 sources
funding Neutral

Cathie Wood’s ARK Invest Doubles Down on CRISPR Therapeutics Amid Market Dip

ARK Invest, led by Cathie Wood, has significantly increased its position in CRISPR Therapeutics (CRSP), signaling continued high conviction in the gene-editing pioneer despite recent market fluctuations. This move highlights Wood's strategy of doubling down on disruptive genomic technologies during periods of valuation compression.

2 sources
gene-therapy Very Bullish

B.C. Teen Becomes First in World Cured of Rare Disease via Gene Editing

A British Columbia teenager has achieved a historic medical milestone, becoming the first person globally to be cured of a rare genetic disease using advanced gene editing technology. This breakthrough marks a definitive shift in the treatment of rare disorders, moving from chronic management to a potential one-time curative intervention.

2 sources