Internal Reference · Policy Intelligence
Prescription Drug Affordability Boards
Knowledge base on state PDABs
Compiled July 28, 2026

1. What is a PDAB?

A Prescription Drug Affordability Board (PDAB) is a state-level body created by legislation to review high-cost prescription drugs, determine which are "unaffordable" to consumers, and — depending on the state — set binding price caps known as Upper Payment Limits (UPLs). States have established PDABs because federal law imposes almost no ceiling on what a manufacturer may charge, leaving price intervention largely to the states.

As of July 2026, nine states have active PDAB statutes, though their powers vary considerably; only four can cap a drug's price — and on July 1, 2026 a federal court blocked the first cap ever adopted.

Core distinction
Not all PDABs can set price caps. A PDAB is the body that reviews drugs and identifies affordability problems; UPL authority is the additional power, conferred by statute, to cap prices. The two are granted separately and do not always come together.

2. How state PDABs formed

Maryland established the first PDAB in 2019. Additional states followed between 2021 and 2024 — most as review-and-recommend boards, four with full UPL authority. Two early boards, New Hampshire and Ohio, were repealed in 2025. The first binding price caps were adopted in 2025–2026, each with a delayed effective date. The nine boards active today, in order of creation:

2019MDFirst in the nation · UPL authority
2019ME
2021NY
2021CO
2021OR
2022WA
2023MN
2023NJ
2024MA
UPL authority Review / transparency only

Boards that were repealed

New Hampshire — enacted 2020 (HB 1280, RSA 126-BB), repealed 7/1/2025; no reviews completed.
Ohio — enacted 2019 (HB 166, ORC § 125.95), advisory-only and dormant since 2021, repealed 7/1/2025.

How UPL authority gets granted

UPL authority is conferred by state legislation: the legislature must enact a statute that expressly grants the board power to set price caps. All four UPL states acquired it the same way — built into the enabling statute at the outset: Maryland (2019), Colorado (2021), Washington (2022), and Minnesota (2023). Statutory citations appear with each board below.

The alternative route — a review-only board amending its statute to add cap authority after the fact — remains untested; no state has completed it. Maine is the furthest along: LD 697 (enacted January 7, 2026) directs its board to recommend UPL authority, which follow-up legislation could grant in 2027. Maine therefore remains a review/report board, and the number of UPL states stands at four.

Why the numbers stay small

Enactment is rarely the obstacle; the politics are. Two distinct thresholds account for the totals — why only nine states have established a PDAB, and why only four hold cap authority:

  1. Establishing any PDAB requires a Democratic trifecta willing to legislate on drug pricing. All nine PDAB states are Democratic trifectas; no Republican-led state has enacted one. Even supportive states stall: Virginia's bill has been vetoed three years running — twice by Gov. Youngkin (R, 2024–25) and again by Gov. Spanberger (D) in May 2026.
  2. Adding UPL cap authority clears a higher threshold. PhRMA, BIO, and state pharmacy associations oppose binding price caps most forcefully; only four of the nine boards hold that power, and none has added it since 2023.

3. Board authority and profiles

The nine active boards divide into two groups by the authority they hold — those that can cap a price, and those limited to review or reporting:

  • PDAB + UPL — reviews a drug, declares it unaffordable, and sets a binding Upper Payment Limit on what carriers, pharmacies, and providers pay. Four boards: Colorado, Maryland, Minnesota, Washington.
  • PDAB only — reviews and/or reports on drug prices but cannot set a binding cap. Five boards: New York, Oregon, Maine, Massachusetts (review/report) and New Jersey (transparency only).

PDAB + UPL authority

MarylandEst. 2019 · UPL authority
Established
2019, codified at Md. Code, Health-General § 21-2C — the first PDAB in the nation. Operates alongside an advisory Stakeholder Council.
Structure
5 voting members appointed by the Governor and legislative leaders, with health-economics or clinical expertise.
Authority
Affordability review plus full Upper Payment Limit (UPL) authority. The 2025 expansion law (SB 357 / HB 424, Ch. 610) extends UPLs from state/local government plans to all payers — contingent on specified actions by Sept 30, 2030 — and adds 340B-impact, FDA-shortage, and Medicaid-consultation checks.
Litigation
None filed against Maryland's UPLs as of July 2026 — but Colorado's July 1 injunction rests on patent preemption, a theory that would reach Maryland's caps equally. Implementation and monitoring regulations were published in the June 12, 2026 Maryland Register; comments closed July 13, 2026.
ColoradoEst. 2021 · UPL authority
Established
2021 via SB21-175, codified at § 10-16-1401 et seq., C.R.S. — Colorado's first body able to set binding drug-price caps. Supported by the Prescription Drug Affordability Advisory Council (PDAAC).
Structure
5 voting members appointed by the Governor and legislative leaders, with health-economics or clinical expertise.
Authority
Affordability review plus full UPL authority. Eligibility: wholesale cost over $30,000/yr, or a price increase over 200% or $3,000 in 12 months. UPLs apply to pharmacy/provider purchases and commercial + state-employee plan reimbursement (not Medicare/Medicaid); enforced by the Colorado Attorney General. A statutory QALY ban bars QALY-based research.
Litigation
Enbrel UPL preliminarily enjoined July 1, 2026. Amgen II — filed Oct 30, 2025 (D. Colo.) on Dormant Commerce Clause and IRA-preemption grounds. Chief Judge Daniel D. Domenico granted a preliminary injunction on a different theory than the one pleaded first: federal patent law preemption, following Federal Circuit precedent striking down the District of Columbia's price-control law. The injunction holds until the case is resolved. Amgen I (state court) dismissed April 2025, dropped on appeal Jan 2026.
WashingtonEst. 2022 · UPL authority
Established
2022 via Second Substitute SB 5532 (Ch. 153, Laws of 2022), codified at Ch. 70.405 RCW.
Structure
5 members (health-economics or clinical expertise) appointed by the Governor, supported by Health Care Authority (HCA) staff; advised by a Core Advisory Group and a drug-specific Supplemental Advisory Group.
Authority
Affordability review plus full UPL authority, but time-gated — no UPL may take effect before Jan 1, 2027, and the Board may cap up to 12 drugs per year. Methodology expected to follow Maryland's model.
Litigation
None to date.
MinnesotaEst. 2023 · UPL authority
Established
2023, codified at Minn. Stat. §§ 62J.84–62J.95; Board formally established effective Jan 1, 2024.
Structure
7 voting members appointed by the Governor, plus 2 nonvoting legislative appointees; advised by the Prescription Drug Affordability Advisory Council. Staffed by the Department of Commerce.
Authority
Affordability review plus full UPL authority. Uniquely, where a drug carries a Medicare Maximum Fair Price, statute requires the UPL to equal that MFP — the only post-IRA PDAB to codify this. No drug selected for review yet.
Litigation
None to date.

How a UPL gets adopted

Granting authority is a one-time legislative act; setting an individual cap is a separate, repeatable process the board conducts itself:

  1. The board selects a drug and conducts an affordability review against statutory cost thresholds.
  2. The board adopts the UPL administratively, through rulemaking rather than new legislation. In Maryland, the board's UPL action plan must first be approved by the Legislative Policy Committee; Colorado and other states set caps through standard agency rulemaking.
  3. A delayed effective date applies. All three UPLs adopted to date (CO–Enbrel, MD–Jardiance, MD–Ozempic) take effect January 1, 2027; none is yet binding on payers.
  4. Litigation can stop it before it starts. The delay between adoption and effect is exactly the window in which a manufacturer sues. Colorado's Enbrel cap was enjoined on July 1, 2026 — six months before it would have bound anyone.
The patent-preemption problem
The Colorado ruling did not turn on the arguments most observers were tracking. Amgen pleaded the Dormant Commerce Clause and IRA preemption; the court enjoined the cap on federal patent law instead, reasoning that a state ceiling on a patented drug's price undercuts the exclusivity federal patent law grants. If that reasoning holds on appeal, it is not a Colorado problem. It applies to any state cap on any patented drug, which is nearly every drug a PDAB would want to reach — and it would not be cured by better methodology or a different statute.

What a UPL actually reaches

Once a cap takes effect, federal law limits its reach. A UPL cannot apply to Medicare beneficiaries (governed by federal Part D) or directly bind Medicaid (governed by federal Medicaid rules). It is also open to two distinct preemption attacks: the IRA theory, that federal Medicare drug-price negotiation already occupies the field; and the patent theory, that capping the price of a patented drug conflicts with the exclusivity federal patent law confers. Colorado's Amgen II suit pleaded the first and won on the second.

A UPL does reach state-employee health plans, commercial insurance sold in the state, and pharmacy and provider purchases — roughly 30–40% of a drug's volume in the state. Significant, but not comprehensive.

PDAB only

These boards can review and recommend but cannot set a price cap, which does not render them inconsequential. Oregon took up Keytruda at its July 15, 2026 review; no determination has been published yet. Absent UPL authority, no binding cap follows even if the board declares the drug unaffordable; the determination nonetheless carries weight. An unaffordability finding becomes a reference point other states cite, increases pressure on the Oregon legislature to grant UPL authority in a future session, and establishes methodology precedent applicable in Colorado, Maryland, and Washington.

MaineEst. 2019 · Review/report
Established
2019 via P.L. 2019, chs. 471–472, codified at Title 5, Ch. 167 (5 M.R.S. §§ 2041–2042). Housed in the Office of Affordable Health Care (OAHC).
Structure
5 voting members on staggered 5-year terms (2 Senate, 2 House, 1 Governor appointees), plus a 12-member advisory council.
Authority
Sets annual spending targets for public-payer drug spending and makes policy recommendations to the Legislature. No price-cap authority. LD 697 (law Jan 2026) directs the board to recommend UPL authority — a 2027 bill could grant it.
Litigation
None — no UPL set.
New YorkEst. 2021 · Review/report
Established
New York runs two parallel boards, not one unified PDAB. The DFS Drug Accountability Board (DAB) was created by Ch. 828 of the Laws of 2021 (Insurance Law § 202); the Medicaid Drug Utilization Review Board (DURB) operates under Social Services Law § 369-bb.
Structure
DAB — experts appointed by the DFS Superintendent. DURB — clinical board chaired by the Medicaid Medical Director, staffed by the Department of Health.
Authority
Two review-and-recommend levers — Medicaid supplemental rebates (DURB) and commercial price determinations (DAB). No price-cap authority. Two commercial price reductions achieved to date via confidential supplemental-refund agreements.
Litigation
None — no UPL in force.
OregonEst. 2021 · Review/report
Established
2021, codified at Ch. 646A ORS (core provisions ORS 646A.689–646A.703). Housed in DCBS, Division of Financial Regulation (DFR).
Structure
8 members appointed by the Governor and confirmed by the Senate (no manufacturer financial ties); meets at least every six weeks.
Authority
Affordability reviews of high-cost drugs and insulin, plus policy recommendations to the Legislature. No price-cap authority. A 2025 law caps reviews at 9 drugs + 1 insulin product per cycle (from 2026).
Litigation
None — no UPL set.
New JerseyEst. 2023 · Transparency only
Established
2023 via P.L. 2023, c. 106 (Prescription Drug Affordability and Transparency Law), codified at N.J.S.A. 45:14-82.11. The Drug Affordability Council sits "in, but not of" the Department of Law & Public Safety; staffed by the Division of Consumer Affairs' Drug Affordability Unit.
Structure
A council of public members and alternate public members (one public seat currently vacant).
Authority
Advisory only. Reviews the state's annual drug-price transparency data and recommends policy to the Governor and Legislature. Cannot review named drugs and has no UPL authority.
Litigation
None — no UPL, no affordability determinations.
MassachusettsEst. 2024 · Review/report
Established
Chapter 342 of the Acts of 2024 (signed Jan 8, 2025) created the Office of Pharmaceutical Policy & Analysis (OPPA), operating from 2025. A separate HPC drug-pricing-review power supporting MassHealth dates to 2018.
Structure
OPPA sits within the Health Policy Commission (independent agency, 11-member board) and functions as the state's pharmaceutical-policy analysis hub rather than a standalone board.
Authority
Data analysis/reporting, plus drug-pricing review on MassHealth referral (assesses whether a price is unreasonable relative to value). Review is Medicaid-triggered and exception-based — only after a failed rebate negotiation and cost above $25,000/utilizer/yr or $10M aggregate. No UPL authority.
Litigation
None — no UPL set.

4. Where things stand, 2025–2026

Current counts

MetricMarch 2025July 2026
States with active PDAB statute119
States with UPL authority44 (unchanged since 2023)
UPLs formally adopted03 (CO-Enbrel, MD-Jardiance, MD-Ozempic)
UPLs operationally in effect00 (remaining two effective 1/1/2027)
UPLs blocked by a court01 (CO-Enbrel, enjoined 7/1/2026)
UPL frameworks advancing03 (MD: Trulicity, Farxiga; CO: Cosentyx)
States with pending PDAB litigation01 (CO – Amgen II)
States that repealed PDAB2 (NH, OH)

The first price caps

No UPL is yet operationally in effect — all carry delayed effective dates — and the first one adopted has now been blocked in court:

  • Oct 2025 — Colorado, Enbrel. First UPL in the nation ($600 per 50mg, roughly $31,000 a year against a current cost near $58,000); was to take effect Jan 1, 2027. Preliminarily enjoined July 1, 2026 and not currently enforceable.
  • Apr 2026 — Maryland, Jardiance. Second UPL (~$204 per 30-day supply, set at the Medicare Maximum Fair Price); effective Jan 1, 2027.
  • May 18, 2026 — Maryland, Ozempic. Third UPL ($274 per 30-day supply, also at MFP, state/local government plans); effective Jan 1, 2027.

The pattern that matters is the sequencing. Adoption is not the milestone it appeared to be nine months ago; the effective date is, and nothing has reached one yet. A cap adopted in October 2025 was still unenforceable in July 2026, and is now blocked indefinitely.

Legislation in flight

StateDevelopmentStatus
VirginiaPDAB-with-UPL bill (SB 271 / HB 483) passed the legislatureVetoed by Gov. Spanberger, 5/19/2026 — third veto in three years
IllinoisSB 3496 would have created a PDAB with UPL authorityDied 5/31/2026. Passed the House 62–39 on 5/22 but the Senate never took it up before adjournment. Gov. Pritzker had said he would sign it; expected to return in 2027.
MaineLD 697 directs the PDAB to recommend UPL authorityEnacted 1/7/2026; recommendation pending

5. State-by-state summary

All nine active PDAB states have Democratic trifectas — a Democratic governor and Democratic control of both legislative chambers.

State Est. UPL Auth Tier Drug pipeline Watch
Maryland 2019 Yes Operational Jardiance (~$204) & Ozempic ($274, gov plans) UPLs adopted · Farxiga next, at MFP ($178.50/30-day) · Trulicity in policy review · Dupixent + Skyrizi queued Every cap set at the Medicare MFP. Now the furthest-advanced program, and the one most exposed if patent preemption holds.
Colorado 2021 Yes Operational Enbrel UPL adopted ($600/50mg) but enjoined 7/1/2026 · Cosentyx in rulemaking · Stelara pre-rulemaking The national test case. A patent-preemption ruling here would reach every state's caps, not just Colorado's.
Washington 2022 Yes Building Selected: Enbrel, Xtandi, Cabometyx, Humira · Enbrel and Xtandi reviews under way; determinations pending Statute bars any UPL before 1/1/2027, so the Colorado ruling lands before Washington can cap anything.
Minnesota 2023 Yes Building No drugs selected yet · governance still building First drug selections expected late 2026.
Maine 2019 No (UPL recommendation only) Pre-pipeline No active reviews Possible UPL expansion in the 2027 session.
New York 2021 No (review + rebate levers) Review active DAB reviews high-cost commercial drugs · DURB negotiates Medicaid supplemental rebates · 2 commercial price cuts to date Manufacturer price-reporting in effect since June 2024; active review levers, but no UPL.
Oregon 2021 No Review-heavy 9+ drugs determined unaffordable · Keytruda reviewed 7/15/2026; determination not yet published First oncology drug at any PDAB. No cap authority, but the finding becomes methodology precedent elsewhere.
New Jersey 2023 No (data/policy only) Dormant Dormant on drug reviews · first PDAC report due 2026 Initial report may alter the state's posture.
Massachusetts 2024 No (referral-based review only) Review-only No publicly named 2026 review OPPA established 2025 under the HPC; lower priority at present.

Sources