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Sit-rep: WatchVAX-014

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Stellis Vaccines · VAX-014

Respiratory syncytial virus in older adults

Adjuvanted RSV vaccine Ph2b dose-finding. Enrolment on plan, but a manufacturing lot deviation triggered a 6-week pause to re-qualify; recovery plan in place.

Phase 2bEnrollingVaccines / Infectious diseaseWatch

Sit-rep

Status

Enrolling

Health

Watch

Forecast end

Dec 11, 2027

+42d vs plan

Projected EAC

22.8M USD

+1.4M USD vs contract

Live activity

No activity yet

Key performance indicators

Threshold colour is supplementary to the on-target / at-risk / breached label.

Enrolment
420 / 600 (70%)
+1% vs planon-target
Screen failure rate
14%
+2 ptson-target
Query aging (>14d)
29 open
+11at-risk
Protocol deviations
37
+12at-risk
Projected DBL variance
+42 days
no recent deltaat-risk
Budget burn
58%
+5 ptson-target
Forecast EAC
$22.8M
+$1.4Mat-risk

Timeline & milestones

Bar shows planned span; tick marks current forecast end. Markers are colour-coded by milestone status (labels in tooltip / table below).

FPI — Complete (2024-12-22)25% enrolment — Complete (2025-05-08)50% enrolment — Complete (2025-10-21)75% enrolment — In progress (2026-04-15)LPI — Planned (2026-10-12)LPLV — Planned (2027-04-11)Database lock — Planned (2027-07-11)CSR draft — Planned (2027-09-26)CSR final — Planned (2027-12-11)
Dec 15, 2024planned end Oct 30, 2027 · forecast end Dec 11, 2027
MilestonePlannedActual / forecastVarianceStatus
FPIDec 15, 2024Dec 22, 2024+7dComplete
25% enrolmentApr 30, 2025May 8, 2025+8dComplete
50% enrolmentSep 30, 2025Oct 21, 2025+21dComplete
75% enrolmentFeb 28, 2026Apr 15, 2026+46dIn progress
LPIAug 30, 2026Oct 12, 2026+43dPlanned
LPLVFeb 28, 2027Apr 11, 2027+42dPlanned
Database lockMay 30, 2027Jul 11, 2027+42dPlanned
CSR draftAug 15, 2027Sep 26, 2027+42dPlanned
CSR finalOct 30, 2027Dec 11, 2027+42dPlanned
SeverityTitleOwnerMitigationStatus
HighManufacturing lot deviation on adjuvant lot ADJ-2025-04CMC LeadLot quarantined; re-qualified replacement lot deployed; CAPA in regulatory review.Mitigating
MediumReactogenicity rate slightly above comparatorMedical MonitorIndependent DSMB review at 50% enrolment: continue unchanged.Closed
LowSeasonal enrolment dip projected through Q3CRA ManagerSouthern hemisphere sites in start-up to offset.Mitigating
MediumCentral lab assay validation re-run required after method updateLab LeadRe-run scheduled; analytical bridge plan agreed.Open

Resources

RoleHeadcountFTEMonthly rateMonthly cost
CRA75.519k USD103k USD
Data Management43.015k USD46k USD
Pharmacovigilance31.618k USD29k USD
Biostatistics21.522k USD33k USD
Medical Writing10.420k USD8k USD
CMC / Manufacturing21.024k USD24k USD
Total1913.0243k USD

Financials

Contracted budget

21.4M USD

EBV spent

12.4M USD

58% of contract

EAC (estimate at completion)

22.8M USD

+1.4M USD vs contract

Burn vs time elapsed

58% / 50%

broadly aligned

Recent activity

Provenance events (24h)

354

Staging items pending

11

Signatures (7d)

27

View provenance for this study →View staged records for this study →

Study goals

  • Establish dose-response for adjuvanted prefusion-F antigen

  • Show seroresponse ≥ 4x baseline in ≥ 80% of subjects per dose

  • Maintain reactogenicity profile comparable to comparator

  • Generate evidence package supporting Ph3 advancement decision