8-K ·Filed Jun 11, 2026

CRBU

Caribou Biosciences, Inc.
BULLISH
Impact 6/10
Horizonmonths Processed3mo ago SEC0001619856-26-000043
8-K context-dependent: Items 7.01, 8.01
Actionable Insight ▲ Bullish

The vispa-cel 2L LBCL data (82% ORR, 17.1-month mPFS) strengthen the case for the pivotal ANTLER-3 phase 3 trial, which targets an underserved patient population. The CB-011 MM data (83% CR, early signal in BCMA-exposed patient) de-risks the dose expansion readout expected in H2 2026. Monitor for initial CB-011 dose expansion data in BCMA-naïve and -exposed patients in late 2026, which will be the next meaningful catalyst. Cash runway and ability to fully fund ANTLER-3 remain key risks not addressed in this filing.

DirectionBullish
Confidencehigh
Horizonmonths
Latest settled — T+20d ⚠ clustered
CRBU ▲ +16.87% at T+20d
LONG call ✓ call won +16.87% · α vs SPY +14.98% · entry $1.66 → $1.94
Next anchor: T+60d due 24d ago
Latest observation: T+56 +14.65% FF3 residual α
Entry anchored
Jun 10, 03:59 PM ET
via exchange tick
T+1d
-3.92%
call -3.92% · α -4.46%
$1.60
settled 4mo ago
T+5d
-1.20%
call -1.20% · α -1.64%
$1.64
settled 4mo ago
T+20d
+16.87%
call +16.87% · α +14.98%
$1.94
settled 3mo ago
T+60d
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call — · α —
—
due 24d ago

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Executive Summary

Caribou Biosciences announced long-term follow-up data from its ANTLER phase 1 (vispa-cel, anti-CD19) and CaMMouflage phase 1 (CB-011, anti-BCMA) trials at the EHA 2026 meeting. For vispa-cel in 2L LBCL (pivotal subgroup, N=27): 82% ORR, 67% CR, 17.1-month mPFS. For CB-011 in r/r MM (BCMA-naïve RDE cohort, N=12): 92% ORR, 83% CR, 91% MRD negativity. Both assets showed manageable safety profiles. The company also reiterated FDA alignment on the design of the ANTLER-3 pivotal phase 3 trial for vispa-cel. This data update is a notable but incremental catalyst for this pre-revenue clinical-stage biotech—positive efficacy readouts but from small, single-arm cohorts without financial guidance.

Key Facts

  • Vispa-cel in 2L LBCL (pivotal optimized subgroup, N=27): 82% ORR, 67% CR rate, 17.1-month median PFS
  • CB-011 in BCMA-naïve r/r MM at RDE (N=12): 92% ORR, 83% CR rate, 91% MRD negativity in 10/11 evaluable, 50% in CR at 15 months
  • CB-011 case study: 71-yo male with 8 prior lines (including autologous CAR-T) achieved CR at day 28, ongoing
  • No GvHD or Gr≥3 ICANS in both pivotal optimized vispa-cel subgroup (N=27) and CB-011 RDE cohort (N=12)
  • FDA alignment reached on ANTLER-3 phase 3 design (~250 patients, 2L LBCL not eligible for transplant/auto-CAR-T, PFS primary endpoint)
  • Initial dose expansion data for CB-011 in BCMA-naïve and -exposed patients expected H2 2026

Financial Impact

No revenue; company is pre-commercial. Data update supports pipeline valuation for vispa-cel and CB-011, two allogeneic CAR-T candidates with FDA RMAT, Fast Track, and Orphan Drug designations.

Risk Factors

  • Company has a history of net operating losses and needs additional capital to fund operations and the ANTLER-3 phase 3 trial
  • Phase 1 data from small single-arm cohorts may not be predictive of phase 3 outcomes or regulatory approval
  • Two treatment-related deaths reported across both trials (one vispa-cel-related IEC-HS, one CB-011-related hematotoxicity)
  • Pre-revenue biotech with high cash burn and dilutive financing risk

Market Snapshot

Exchange
Nasdaq
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
93% bullish (14 analysts)

Investment Themes

Biotech & Drug Discovery

Documents Analyzed

This report is based on 6 SEC documents filed with EDGAR.

DocumentAccession Number
8-K Filing (Primary)0001619856-26-000043
Document: crbu-20260611xexx992.htm0001619856-26-000043
Document: crbu-20260611xexx991.htm0001619856-26-000043
Document: 0001619856-26-000043-index-headers.html0001619856-26-000043
Document: 0001619856-26-000043-index.html0001619856-26-000043
Document: 0001619856-26-000043.txt0001619856-26-000043
10 reports for CRBU
Performance horizon

Track record builds as more directional reports settle.

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Reports for CRBU — sortable, filterable
TypeNow
Jun 11, 2026
16w ago
8-K
BULLISH ★ 6/10
$1.66 $1.94▲ +16.87%▲ +14.98%$1.23 (−26.20%)
Jun 11, 2026
16w ago
Press Release
BULLISH ★ 7/10
$1.66 $1.94▲ +16.87%▲ +14.98%$1.23 (−26.20%)
Jun 5, 2026
16w ago
DEFA14A
NEUTRAL ★ 2/10
$1.84 $1.83▼ −0.54%▼ −2.17%$1.23 (−33.42%)
Apr 24, 2026
22w ago
DEFA14A
NEUTRAL ★ 3/10
$2.13 $2.16▲ +1.41%▼ −3.55%$1.23 (−42.49%)
Mar 5, 2026
30w ago
8-K
MIXED ★ 5/10
$1.82 $1.95▲ +7.14%▲ +9.19%$1.23 (−32.69%)
Mar 5, 2026
30w ago
Press Release
MIXED ★ 6/10
$1.82 $1.95▲ +7.14%▲ +9.19%$1.23 (−32.69%)
Feb 28, 2026
30w ago
Institutional Cluster
NEUTRAL ★ 5/10
$1.84 $1.72▼ −6.52%▲ +1.42%$1.23 (−33.42%)
Feb 24, 2026
31w ago
Insider Cluster
NEUTRAL ★ 3/10
$2.14 $1.82▼ −14.95%▼ −9.97%$1.23 (−42.76%)
Feb 24, 2026
31w ago
Insider Cluster
NEUTRAL ★ 4/10
$2.14 $1.82▼ −14.95%▼ −9.97%$1.23 (−42.76%)
Feb 24, 2026
31w ago
Insider Cluster
NEUTRAL ★ 3/10
$2.14 $1.82▼ −14.95%▼ −9.97%$1.23 (−42.76%)
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