Cambridge biotech tracker · Cambridge

Moderna

Listed on Nasdaq as MRNA, filed under SEC industry code 2836 (biological products). Fiscal year ends in December. Numbers below are from the company’s own SEC filings through Q2 '26.

Cash & investments
$6.91B
Q2 '26 · Jun 30, 2026
Burn per quarter
$268M
avg. operating cash flow, 4 qtrs
Runway
5+ yrs
3+ years
Net loss
$782M
Q2 '26
R&D expense
$651M
68% of opex
Raised, last 4 qtrs
+$611M
net financing cash flow
Next readout
Feb 2027
Phase 3 · cash past the catalyst

Cash & investments

Quarter-end balance

Cash & investments$0$5B$10BQ3 '24Q4 '24Q1 '25Q2 '25Q3 '25Q4 '25Q1 '26Q2 '26$6.91B$9.52B

Operating cash flow

Per quarter; below zero is burn

Operating cash flow−$2B−$500M$1B$0Q3 '24Q4 '24Q1 '25Q2 '25Q3 '25Q4 '25Q1 '26Q2 '26−$526M−$1.57B

R&D expense

Per quarter

R&D expense$0$1B$2BQ3 '24Q4 '24Q1 '25Q2 '25Q3 '25Q4 '25Q1 '26Q2 '26$651M$1.14B

Two views of the runway

Compare across the cluster

The outside view

5+ years

Cash at Q2 '26 divided by the average burn of the last four quarters, $89.4M a month.

Management’s own date

12+ months

The latest filing states only the going concern minimum, that cash covers at least twelve months from issuance. No sharper date was filed.

Cash against the calendar

What the runway has to reach.

Next expected readoutPhase 3

Feb 2027estimated

A Study to Investigate the Safety and Efficacy of mRNA-1403 in Participants ≥18 Years of Age for the Prevention of Acute Gastroenteritis

Acute Gastroenteritis · Norovirus Acute Gastroenteritis

NCT06592794 on ClinicalTrials.gov

Does the cash reach it?

Cash past the catalyst

Runway
5+ years
Time to the date
3 months

It is about 3 months out. At the current burn there is roughly 74 months of cash left on the far side of it, which is enough room to raise on the result rather than ahead of it.

Pipeline

24 active trials, through phase 4.

Phase 1 · 10Phase 1/2 · 7Phase 2 · 5Phase 4 · 4Phase 3 · 2

Study
A Study of Updated mRNA Seasonal Influenza VaccinesNCT07884175 · Seasonal InfluenzaPhase 4Dec 2026est.· not a catalyst
A Study to Investigate the Immunogenicity and Safety of mRNA COVID-19 Variant-containing FormulationsNCT07863635 · SARS-CoV-2Phase 4Dec 2026est.· not a catalyst
A Study to Investigate the Immunogenicity and Safety of mRNA COVID-19 Variant-containing Vaccine FormulationsNCT06585241 · SARS-CoV-2Phase 4Dec 2026est.· not a catalyst
A Study to Evaluate the Efficacy and Safety of mRNA-1283 and mRNA-1273 in Participants 50 to 64 Years of Age Without High-Risk Conditions for Severe Coronavirus Disease 2019 (COVID-19)NCT07266558 · SARS-CoV-2Phase 4Jun 2027est.· not a catalyst
A Study of mRNA-1018-H5 Pandemic Influenza Vaccine in Healthy AdultsNCT07496450 · InfluenzaPhase 3Jan 2027est.· not a catalyst
A Study to Investigate the Safety and Efficacy of mRNA-1403 in Participants ≥18 Years of Age for the Prevention of Acute GastroenteritisNCT06592794 · Acute Gastroenteritis, Norovirus Acute GastroenteritisPhase 3Feb 2027est.
A Study to Evaluate the Efficacy, Safety, and Immunogenicity of mRNA-1647 Cytomegalovirus (CMV) Vaccine in Allogenic Hematopoietic Cell Transplantation (HCT) Participants.NCT05683457 · Cytomegalovirus InfectionPhase 2Mar 2027est.
A Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1982 to Prevent Lyme Disease in Healthy Participants (18 to 70 Years of Age)NCT07561294 · Lyme DiseasePhase 2Nov 2028est.· not a catalyst
A Study to Investigate Multiple Sclerosis Relapse Prevention With mRNA-1195 Compared With Placebo in Participants Aged 18 to ≤55 YearsNCT06735248 · Multiple SclerosisPhase 2Jan 2029est.
A Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1283 in Participants ≥6 Months to <12 Years of AgeNCT07808697 · SARS-CoV-2Phase 2Aug 2029est.
An Efficacy Study of Adjuvant Treatment With the Personalized Cancer Vaccine mRNA-4157 and Pembrolizumab in Participants With High-Risk Melanoma (KEYNOTE-942)NCT03897881 · MelanomaPhase 2Nov 2032est.
A Study of an Epstein-Barr Virus (EBV) Candidate Vaccine, mRNA-1189, in 10- to 30-Year-Old Healthy Adolescents and AdultsNCT05164094 · Epstein-Barr Virus InfectionPhase 1/2Oct 2026est.
A Study of mRNA-3745 in Adult and Pediatric Participants With Glycogen Storage Disease Type 1a (GSD1a)NCT05095727 · Glycogen Storage DiseasePhase 1/2Nov 2026est.
Open-Label Study of mRNA-3927 in Participants With Propionic AcidemiaNCT04159103 · Propionic AcidemiaPhase 1/2Aug 2027est.
A Study to Assess the Long-term Safety and Clinical Activity of mRNA-3927 in Participants Previously Enrolled in the mRNA-3927-P101 StudyNCT05130437 · Propionic AcidemiaPhase 1/2Dec 2029est.· not a catalyst
A Study of mRNA-2808 in Participants With Relapsed or Refractory Multiple MyelomaNCT07116616 · Relapsed or Refractory Multiple MyelomaPhase 1/2Jun 2030est.
Study of mRNA-4359 Administered Alone and in Combination With Immune Checkpoint Blockade in Participants With Advanced Solid TumorsNCT05533697 · Advanced Solid TumorsPhase 1/2Feb 2032est.
An Extension Study to Evaluate the Long-Term Safety and Clinical Activity of mRNA-3705 in Participants Previously Enrolled in Other Clinical Studies of mRNA-3705NCT05295433 · Methylmalonic AcidemiaPhase 1/2Apr 2034est.· not a catalyst
A Study to Investigate Safety and Tolerability of mRNA-0184 Administered Subcutaneously in Healthy ParticipantsNCT06655870 · Healthy ParticipantsPhase 1Dec 2026est.· not a catalyst
A Study of an Epstein-Barr Virus (EBV) Candidate Vaccine, mRNA-1189 in Healthy Adults 18 to 30 Years of AgeNCT07478952 · Epstein-Barr VirusPhase 1May 2027est.· not a catalyst
A Study to Investigate Safety, Reactogenicity, and Immunogenicity of mRNA-1365 (Profile 2) in Older Healthy AdultsNCT07764237 · Respiratory Syncytial Virus (RSV), Human Metapneuomovirus (hMPV)Phase 1Jul 2027est.· not a catalyst
A Study of mRNA-4106 or mRNA-4200 Administered Alone or in Combination With Anti-Cancer Agents in Participants With Solid TumorsNCT06880549 · Advanced Solid TumorsPhase 1Aug 2027est.
A Study to Investigate the Safety, Reactogenicity, and Immunogenicity of mRNA-1469 Vaccine to Prevent Ebola-Bundibugyo Virus Disease in Healthy Adult ParticipantsNCT07737717 · Ebola-Bundibugyo Virus Disease (Ebola-BDBV)Phase 1Sep 2027est.· not a catalyst
Safety, Tolerability, and Immunogenicity of mRNA-4157 Alone and in Combination in Participants With Solid TumorsNCT03313778 · Solid TumorsPhase 1Nov 2027est.

Interventional studies where this company is the lead sponsor, from ClinicalTrials.gov. Primary completion is when the last patient is measured on the primary endpoint, which is when the data exists rather than when it is announced. Extension, rollover and healthy-volunteer studies are listed but marked as non-catalysts, because they finish long after the result that mattered. Sponsors revise these dates as enrollment moves, so an estimate is a plan rather than a promise.

The controller’s read

What the filings say.

Generated from the numbers above using the same questions I ask when I open a client’s books: how long the cash lasts, what is driving the gap between loss and burn, and where the accounting judgment sits.

Get this read on your company

The cash clears the next catalyst

The next dated event is a phase 3 readout in Feb 2027, about 3 months out. That leaves roughly 74 months of cash afterwards, which is the position you want: the raise can be negotiated on the data instead of on the calendar.

About 5+ years of runway

Cash and investments of $6.91B at Q2 '26 against an average operating cash burn of $268M per quarter over the last four reported quarters runs out around November 2032. More than two years of runway means the finance conversation is about deployment, not survival.

Cash position down $2.29B since Q3 '24

Net financing inflows of $611M over the last four quarters, from equity, debt, or ATM sales, partly offset operating burn. The balance is the number the board watches; the trend is the number the auditors watch.

Net loss runs $256M above cash burn

The Q2 '26 net loss of $782M includes non-cash charges, including $120M of stock-based compensation, that do not consume cash. Burn, not net loss, is what runway is built on.

R&D is 68% of operating expenses

$651M of R&D against $960M of total operating expenses in Q2 '26, with G&A at $216M. For a clinical-stage company, the accounting questions live inside that R&D line: CRO and CMC accruals, milestone recognition, and what gets capitalized versus expensed under ASC 730.

Revenue of $145M in Q2 '26

The balance sheet carries $442M of deferred revenue, which is typically upfront collaboration or license payments being recognized over time. Collaboration and license revenue under ASC 606 and ASC 808 is the single most judgment-heavy area in biotech accounting: performance obligations, variable consideration on milestones, and the split between revenue and cost-sharing.

$591M of long-term debt or convertible notes

Debt in a pre-revenue biotech usually comes with liquidity covenants and, for convertibles, embedded features that need ASC 815 and ASC 470 analysis each quarter.

Retained earnings of $5.10B

Cumulative profits exceed cumulative losses, which puts this company in a different accounting conversation from most of the neighborhood.

Quarterly detail, eight quarters
QuarterCash & inv.Op. cash flowNet incomeR&DG&ARevenueStock compFinancing
Q3 '24 · Sep 30, 24$9.20B−$1.57B$13.0M$1.14B$281M$1.86B$112M$11.0M
Q4 '24 · Dec 31, 24$9.52B$825M−$1.12B$1.12B$351M$966M$104M−$3.0M
Q1 '25 · Mar 31, 25$8.39B−$1.04B−$971M$856M$212M$108M$115M$4.0M
Q2 '25 · Jun 30, 25$7.50B−$919M−$825M$700M$230M$142M$130M$9.0M
Q3 '25 · Sep 30, 25$6.65B−$847M−$200M$801M$268M$1.02B$125M−$1.0M
Q4 '25 · Dec 31, 25$8.13B$930M−$826M$775M$308M$678M$113M$581M
Q1 '26 · Mar 31, 26$7.46B−$630M−$1.34B$649M$173M$389M$104M$17.0M
Q2 '26 · Jun 30, 26$6.91B−$526M−$782M$651M$216M$145M$120M$14.0M

Source: SEC EDGAR XBRL company facts, latest filed value for each period. Fourth quarters are derived from annual less nine-month figures; quarterly cash flows are derived from year-to-date amounts. Not investment advice. If a figure disagrees with the filing, the filing is right.